esv3856598

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:48
Validation:Not tested
Clinical Assertions: No
Region Size:178,262

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: 3114 SVs from 99 studies. See in: genome view

Remapped(Score: Perfect):11,934,533-12,112,794

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3856598	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
esv3856598	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	11,934,533	12,112,794

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv21479054	deletion	HG00155	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,605
essv21479055	deletion	HG00599	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,451
essv21479056	deletion	HG01073	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,366
essv21479057	deletion	HG01384	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,088
essv21479058	deletion	HG01491	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,598
essv21479059	deletion	HG01812	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,403
essv21479060	deletion	HG01813	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,439
essv21479061	deletion	HG01927	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,225
essv21479062	deletion	HG01936	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,302
essv21479063	deletion	HG02298	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,793
essv21479064	deletion	HG02312	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,341
essv21479065	deletion	HG02322	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,722
essv21479066	deletion	HG02379	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,697
essv21479067	deletion	HG02700	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,426
essv21479068	deletion	HG02971	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,790
essv21479069	deletion	HG03111	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,980
essv21479070	deletion	HG03163	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,980
essv21479071	deletion	HG03370	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,015
essv21479072	deletion	HG03388	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,983
essv21479073	deletion	HG03567	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,389
essv21479074	deletion	HG03773	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,605
essv21479075	deletion	HG03824	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,561
essv21479076	deletion	HG04022	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,666
essv21479077	deletion	HG04063	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,140
essv21479078	deletion	HG04134	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,083
essv21479079	deletion	HG04206	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,791
essv21479080	deletion	NA12383	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,473
essv21479081	deletion	NA18544	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,559
essv21479082	deletion	NA18545	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,168
essv21479083	deletion	NA18610	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,407
essv21479084	deletion	NA18626	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,468
essv21479085	deletion	NA18959	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,528
essv21479086	deletion	NA18970	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,526
essv21479087	deletion	NA18983	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,716
essv21479088	deletion	NA18988	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,938
essv21479089	deletion	NA19006	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,645
essv21479090	deletion	NA19067	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,784
essv21479091	deletion	NA19159	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,279
essv21479092	deletion	NA19184	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,210
essv21479093	deletion	NA19222	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,939
essv21479094	deletion	NA19310	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,602
essv21479095	deletion	NA19403	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,594
essv21479096	deletion	NA19446	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,977
essv21479097	deletion	NA19449	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,523
essv21479098	deletion	NA19658	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,523
essv21479099	deletion	NA19834	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,190
essv21479100	deletion	NA20863	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,682
essv21479101	deletion	NA21141	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,407

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv21479054	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479055	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479056	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479057	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479058	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479059	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479060	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479061	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479062	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479063	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479064	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479065	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479066	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479067	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479068	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479069	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479070	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479071	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479072	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479073	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479074	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479075	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479076	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479077	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479078	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479079	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479080	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479081	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479082	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479083	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479084	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479085	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479086	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479087	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479088	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479089	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479090	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479091	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479092	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479093	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479094	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479095	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479096	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479097	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479098	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479099	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479100	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479101	Remapped	Perfect	NC_000009.12:g.119 34533_12112794del	GRCh38.p12	First Pass	NC_000009.12	Chr9	11,934,533	12,112,794
essv21479054	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479055	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479056	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479057	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479058	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479059	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479060	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479061	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479062	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479063	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479064	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479065	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479066	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479067	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479068	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479069	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479070	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479071	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479072	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479073	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479074	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479075	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479076	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479077	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479078	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479079	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479080	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479081	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479082	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479083	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479084	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479085	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479086	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479087	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479088	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479089	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479090	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479091	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479092	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479093	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479094	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479095	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479096	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479097	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479098	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479099	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479100	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794
essv21479101	Submitted genomic		NC_000009.11:g.119 34533_12112794del	GRCh37 (hg19)		NC_000009.11	Chr9	11,934,533	12,112,794

dbVar

Database of genomic structural variation

esv3856598

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.