esv3599101

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:45
Validation:Not tested
Clinical Assertions: No
Region Size:2,463

Publication(s):1000 Genomes Project Consortium et al. 2015

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: 199 SVs from 39 studies. See in: genome view

Remapped(Score: Perfect):191,293,415-191,295,878

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3599101	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
esv3599101	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv11270989	deletion	SAMN00249860	Sequencing	Read depth and paired-end mapping	Heterozygous	2,613
essv11270990	deletion	SAMN00255115	Sequencing	Read depth and paired-end mapping	Heterozygous	3,322
essv11270991	deletion	SAMN00255125	Sequencing	Read depth and paired-end mapping	Heterozygous	3,547
essv11270992	deletion	SAMN00262992	Sequencing	Read depth and paired-end mapping	Heterozygous	3,290
essv11270993	deletion	SAMN00630200	Sequencing	Read depth and paired-end mapping	Heterozygous	3,059
essv11270994	deletion	SAMN00630220	Sequencing	Read depth and paired-end mapping	Heterozygous	3,027
essv11270995	deletion	SAMN00630222	Sequencing	Read depth and paired-end mapping	Heterozygous	3,114
essv11270996	deletion	SAMN00630226	Sequencing	Read depth and paired-end mapping	Heterozygous	3,053
essv11270997	deletion	SAMN00630228	Sequencing	Read depth and paired-end mapping	Heterozygous	3,266
essv11270998	deletion	SAMN00779934	Sequencing	Read depth and paired-end mapping	Heterozygous	3,188
essv11270999	deletion	SAMN00630250	Sequencing	Read depth and paired-end mapping	Heterozygous	2,763
essv11271000	deletion	SAMN01091047	Sequencing	Read depth and paired-end mapping	Heterozygous	2,580
essv11271001	deletion	SAMN01091050	Sequencing	Read depth and paired-end mapping	Heterozygous	2,539
essv11271002	deletion	SAMN01036710	Sequencing	Read depth and paired-end mapping	Heterozygous	3,268
essv11271003	deletion	SAMN01036764	Sequencing	Read depth and paired-end mapping	Heterozygous	2,922
essv11271004	deletion	SAMN01761217	Sequencing	Read depth and paired-end mapping	Heterozygous	2,482
essv11271005	deletion	SAMN01761282	Sequencing	Read depth and paired-end mapping	Heterozygous	3,186
essv11271006	deletion	SAMN01036781	Sequencing	Read depth and paired-end mapping	Heterozygous	3,163
essv11271007	deletion	SAMN01090774	Sequencing	Read depth and paired-end mapping	Heterozygous	3,029
essv11271008	deletion	SAMN01761247	Sequencing	Read depth and paired-end mapping	Heterozygous	3,183
essv11271009	deletion	SAMN01090850	Sequencing	Read depth and paired-end mapping	Heterozygous	2,923
essv11271010	deletion	SAMN01761319	Sequencing	Read depth and paired-end mapping	Heterozygous	3,229
essv11271011	deletion	SAMN01090778	Sequencing	Read depth and paired-end mapping	Heterozygous	2,895
essv11271012	deletion	SAMN01036788	Sequencing	Read depth and paired-end mapping	Heterozygous	3,166
essv11271013	deletion	SAMN01090820	Sequencing	Read depth and paired-end mapping	Heterozygous	3,024
essv11271014	deletion	SAMN01090793	Sequencing	Read depth and paired-end mapping	Heterozygous	2,951
essv11271015	deletion	SAMN01090812	Sequencing	Read depth and paired-end mapping	Heterozygous	2,924
essv11271016	deletion	SAMN00001585	Sequencing	Read depth and paired-end mapping	Heterozygous	3,075
essv11271017	deletion	SAMN00000475	Sequencing	Read depth and paired-end mapping	Heterozygous	3,336
essv11271018	deletion	SAMN00001023	Sequencing	Read depth and paired-end mapping	Heterozygous	3,376
essv11271019	deletion	SAMN00001670	Sequencing	Read depth and paired-end mapping	Heterozygous	3,144
essv11271020	deletion	SAMN00000557	Sequencing	Read depth and paired-end mapping	Heterozygous	2,838
essv11271021	deletion	SAMN00001693	Sequencing	Read depth and paired-end mapping	Heterozygous	3,331
essv11271022	deletion	SAMN00000575	Sequencing	Read depth and paired-end mapping	Heterozygous	3,345
essv11271023	deletion	SAMN00001697	Sequencing	Read depth and paired-end mapping	Heterozygous	3,373
essv11271024	deletion	SAMN00001104	Sequencing	Read depth and paired-end mapping	Heterozygous	2,712
essv11271025	deletion	SAMN00001112	Sequencing	Read depth and paired-end mapping	Heterozygous	2,972
essv11271026	deletion	SAMN00001137	Sequencing	Read depth and paired-end mapping	Heterozygous	3,195
essv11271027	deletion	SAMN00001164	Sequencing	Read depth and paired-end mapping	Heterozygous	2,395
essv11271028	deletion	SAMN00001184	Sequencing	Read depth and paired-end mapping	Heterozygous	2,973
essv11271029	deletion	SAMN00007704	Sequencing	Read depth and paired-end mapping	Heterozygous	2,729
essv11271030	deletion	SAMN00007806	Sequencing	Read depth and paired-end mapping	Heterozygous	3,302
essv11271031	deletion	SAMN00007826	Sequencing	Read depth and paired-end mapping	Heterozygous	2,586
essv11271032	deletion	SAMN00007845	Sequencing	Read depth and paired-end mapping	Heterozygous	2,375
essv11271033	deletion	SAMN00007868	Sequencing	Read depth and paired-end mapping	Heterozygous	2,466

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv11270989	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270990	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270991	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270992	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270993	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270994	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270995	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270996	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270997	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270998	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270999	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271000	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271001	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271002	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271003	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271004	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271005	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271006	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271007	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271008	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271009	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271010	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271011	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271012	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271013	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271014	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271015	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271016	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271017	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271018	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271019	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271020	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271021	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271022	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271023	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271024	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271025	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271026	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271027	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271028	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271029	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271030	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271031	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271032	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11271033	Remapped	Perfect	NC_000003.12:g.(19 1293415_191293416) _(191295877_191295 878)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	191,293,415 (-0, +1)	191,295,877 (-0, +1)
essv11270989	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270990	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270991	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270992	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270993	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270994	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270995	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270996	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270997	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270998	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11270999	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271000	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271001	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271002	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271003	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271004	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271005	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271006	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271007	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271008	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271009	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271010	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271011	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271012	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271013	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271014	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271015	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271016	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271017	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271018	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271019	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271020	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271021	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271022	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271023	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271024	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271025	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271026	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271027	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271028	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271029	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271030	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271031	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271032	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)
essv11271033	Submitted genomic		NC_000003.11:g.(19 1011204_191011205) _(191013666_191013 667)del	GRCh37 (hg19)		NC_000003.11	Chr3	191,011,204 (-0, +1)	191,013,666 (-0, +1)

dbVar

Database of genomic structural variation

esv3599101

Links to Other Resources

Genome View

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.