esv3851084

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:57
Validation:Not tested
Clinical Assertions: No
Region Size:10,297

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 270 SVs from 54 studies. See in: genome view

Remapped(Score: Perfect):118,504,427-118,515,126

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3851084	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
esv3851084	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv20851233	deletion	HG01879	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,099
essv20851234	deletion	HG01883	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,989
essv20851235	deletion	HG01886	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,702
essv20851236	deletion	HG01914	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,133
essv20851237	deletion	HG02281	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,314
essv20851238	deletion	HG02307	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	4,107
essv20851239	deletion	HG02323	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,049
essv20851240	deletion	HG02420	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,119
essv20851241	deletion	HG02450	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,332
essv20851242	deletion	HG02470	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,457
essv20851243	deletion	HG02485	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,523
essv20851244	deletion	HG02502	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,021
essv20851245	deletion	HG02645	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,207
essv20851246	deletion	HG02679	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,914
essv20851247	deletion	HG02769	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,837
essv20851248	deletion	HG02799	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,947
essv20851249	deletion	HG02819	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,025
essv20851250	deletion	HG02820	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,622
essv20851251	deletion	HG02896	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,590
essv20851252	deletion	HG02982	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,258
essv20851253	deletion	HG03027	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,932
essv20851254	deletion	HG03039	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,126
essv20851255	deletion	HG03058	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,870
essv20851256	deletion	HG03072	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,943
essv20851257	deletion	HG03082	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,942
essv20851258	deletion	HG03224	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,231
essv20851259	deletion	HG03258	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,123
essv20851260	deletion	HG03303	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,011
essv20851261	deletion	HG03313	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,432
essv20851262	deletion	HG03382	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,291
essv20851263	deletion	HG03391	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,187
essv20851264	deletion	HG03394	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,416
essv20851265	deletion	HG03439	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	4,090
essv20851266	deletion	HG03460	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,875
essv20851267	deletion	HG03472	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,159
essv20851268	deletion	HG03521	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,340
essv20851269	deletion	HG03548	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,604
essv20851270	deletion	HG03575	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,453
essv20851271	deletion	HG03583	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,621
essv20851272	deletion	NA18517	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,021
essv20851273	deletion	NA18877	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,288
essv20851274	deletion	NA19028	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,879
essv20851275	deletion	NA19037	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,920
essv20851276	deletion	NA19099	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,102
essv20851277	deletion	NA19113	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,015
essv20851278	deletion	NA19171	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,833
essv20851279	deletion	NA19204	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,129
essv20851280	deletion	NA19214	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,493
essv20851281	deletion	NA19248	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,978
essv20851282	deletion	NA19446	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,977
essv20851283	deletion	NA19455	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	3,942
essv20851284	deletion	NA19704	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,768
essv20851285	deletion	NA19707	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,605
essv20851286	deletion	NA19908	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,927
essv20851287	deletion	NA20127	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,044
essv20851288	deletion	NA20291	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,414
essv20851289	deletion	NA20359	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,821

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv20851233	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851234	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851235	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851236	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851237	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851238	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851239	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851240	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851241	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851242	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851243	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851244	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851245	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851246	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851247	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851248	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851249	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851250	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851251	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851252	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851253	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851254	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851255	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851256	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851257	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851258	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851259	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851260	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851261	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851262	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851263	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851264	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851265	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851266	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851267	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851268	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851269	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851270	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851271	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851272	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851273	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851274	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851275	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851276	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851277	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851278	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851279	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851280	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851281	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851282	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851283	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851284	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851285	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851286	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851287	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851288	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851289	Remapped	Perfect	NC_000007.14:g.(11 8504427_118504600) _(118514896_118515 126)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	118,504,600 (-173, +0)	118,514,896 (-0, +230)
essv20851233	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851234	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851235	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851236	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851237	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851238	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851239	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851240	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851241	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851242	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851243	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851244	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851245	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851246	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851247	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851248	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851249	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851250	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851251	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851252	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851253	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851254	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851255	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851256	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851257	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851258	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851259	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851260	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851261	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851262	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851263	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851264	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851265	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851266	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851267	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851268	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851269	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851270	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851271	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851272	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851273	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851274	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)
essv20851275	Submitted genomic		NC_000007.13:g.(11 8144481_118144654) _(118154950_118155 180)del	GRCh37 (hg19)		NC_000007.13	Chr7	118,144,654 (-173, +0)	118,154,950 (-0, +230)

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dbVar

Database of genomic structural variation

esv3851084

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.