esv3827608

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:40
Validation:Not tested
Clinical Assertions: No
Region Size:22,119

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: 266 SVs from 46 studies. See in: genome view

Remapped(Score: Perfect):193,713,242-193,736,360

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3827608	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
esv3827608	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv18028700	deletion	HG00458	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,475
essv18028701	deletion	HG00536	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,664
essv18028702	deletion	HG00542	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,469
essv18028703	deletion	HG00623	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,429
essv18028704	deletion	HG00879	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,220
essv18028705	deletion	HG00881	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,669
essv18028706	deletion	HG01187	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,727
essv18028707	deletion	HG01190	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,469
essv18028708	deletion	HG01342	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,550
essv18028709	deletion	HG01498	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,805
essv18028710	deletion	HG01571	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,745
essv18028711	deletion	HG01805	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,389
essv18028712	deletion	HG01850	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,368
essv18028713	deletion	HG01864	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,552
essv18028714	deletion	HG01893	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,364
essv18028715	deletion	HG01920	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,547
essv18028716	deletion	HG01927	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,225
essv18028717	deletion	HG01953	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,116
essv18028718	deletion	HG01997	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,083
essv18028719	deletion	HG02064	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,488
essv18028720	deletion	HG02075	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,497
essv18028721	deletion	HG02078	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,478
essv18028722	deletion	HG02131	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,490
essv18028723	deletion	HG02153	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,368
essv18028724	deletion	HG02188	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,242
essv18028725	deletion	HG02250	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,687
essv18028726	deletion	HG02252	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,179
essv18028727	deletion	HG02260	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,293
essv18028728	deletion	HG02345	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,758
essv18028729	deletion	HG02386	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,602
essv18028730	deletion	NA18544	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,559
essv18028731	deletion	NA18567	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,379
essv18028732	deletion	NA18573	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,307
essv18028733	deletion	NA18596	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,369
essv18028734	deletion	NA18605	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,715
essv18028735	deletion	NA18740	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,501
essv18028736	deletion	NA18749	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,328
essv18028737	deletion	NA18993	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,206
essv18028738	deletion	NA19090	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,402
essv18028739	deletion	NA19780	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,243

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv18028700	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028701	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028702	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028703	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028704	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028705	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028706	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028707	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028708	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028709	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028710	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028711	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028712	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028713	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028714	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028715	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028716	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028717	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028718	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028719	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028720	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028721	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028722	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028723	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028724	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028725	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028726	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028727	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028728	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028729	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028730	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028731	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028732	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028733	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028734	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028735	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028736	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028737	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028738	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028739	Remapped	Perfect	NC_000002.12:g.(19 3713242_193713742) _(193735860_193736 360)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	193,713,742 (-500, +0)	193,735,860 (-0, +500)
essv18028700	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028701	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028702	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028703	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028704	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028705	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028706	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028707	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028708	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028709	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028710	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028711	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028712	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028713	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028714	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028715	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028716	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028717	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028718	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028719	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028720	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028721	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028722	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028723	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028724	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028725	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028726	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028727	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028728	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028729	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028730	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028731	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028732	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028733	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028734	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028735	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028736	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028737	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028738	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)
essv18028739	Submitted genomic		NC_000002.11:g.(19 4577966_194578466) _(194600584_194601 084)del	GRCh37 (hg19)		NC_000002.11	Chr2	194,578,466 (-500, +0)	194,600,584 (-0, +500)

dbVar

Database of genomic structural variation

esv3827608

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.