esv3625569

Organism: Homo sapiens

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

Variant Calls:56
Validation:Not tested
Clinical Assertions: No
Region Size:30,227

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: 260 SVs from 69 studies. See in: genome view

Remapped(Score: Perfect):21,165,387-21,195,613

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3625569	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
esv3625569	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	21,186,933	21,217,159

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv14047514	copy number loss	SAMN01091086	Sequencing	Read depth and paired-end mapping	Heterozygous	2,326
essv14047515	copy number loss	SAMN00009172	Sequencing	Read depth and paired-end mapping	Heterozygous	2,748
essv14047516	copy number loss	SAMN00014330	Sequencing	Read depth and paired-end mapping	Heterozygous	2,804
essv14047517	copy number loss	SAMN00255125	Sequencing	Read depth and paired-end mapping	Heterozygous	3,547
essv14047518	copy number loss	SAMN00262993	Sequencing	Read depth and paired-end mapping	Heterozygous	3,311
essv14047519	copy number loss	SAMN00262992	Sequencing	Read depth and paired-end mapping	Heterozygous	3,290
essv14047520	copy number loss	SAMN00262968	Sequencing	Read depth and paired-end mapping	Heterozygous	3,187
essv14047521	copy number loss	SAMN00630212	Sequencing	Read depth and paired-end mapping	Heterozygous	3,142
essv14047522	copy number loss	SAMN00262989	Sequencing	Read depth and paired-end mapping	Heterozygous	3,027
essv14047523	copy number loss	SAMN00630222	Sequencing	Read depth and paired-end mapping	Heterozygous	3,114
essv14047524	copy number loss	SAMN00779931	Sequencing	Read depth and paired-end mapping	Heterozygous	3,117
essv14047525	copy number loss	SAMN01091045	Sequencing	Read depth and paired-end mapping	Homozygous	3,089
essv14047526	copy number loss	SAMN01091049	Sequencing	Read depth and paired-end mapping	Heterozygous	2,372
essv14047527	copy number loss	SAMN00630252	Sequencing	Read depth and paired-end mapping	Heterozygous	2,909
essv14047528	copy number loss	SAMN00779945	Sequencing	Read depth and paired-end mapping	Heterozygous	3,175
essv14047529	copy number loss	SAMN00779966	Sequencing	Read depth and paired-end mapping	Heterozygous	3,189
essv14047530	copy number loss	SAMN00779978	Sequencing	Read depth and paired-end mapping	Heterozygous	3,207
essv14047531	copy number loss	SAMN01036713	Sequencing	Read depth and paired-end mapping	Heterozygous	3,109
essv14047532	copy number loss	SAMN01036725	Sequencing	Read depth and paired-end mapping	Heterozygous	3,135
essv14047533	copy number loss	SAMN01036773	Sequencing	Read depth and paired-end mapping	Heterozygous	2,954
essv14047534	copy number loss	SAMN01036775	Sequencing	Read depth and paired-end mapping	Heterozygous	3,028
essv14047535	copy number loss	SAMN01036797	Sequencing	Read depth and paired-end mapping	Heterozygous	3,180
essv14047536	copy number loss	SAMN01090870	Sequencing	Read depth and paired-end mapping	Heterozygous	3,187
essv14047537	copy number loss	SAMN01036755	Sequencing	Read depth and paired-end mapping	Heterozygous	3,248
essv14047538	copy number loss	SAMN01090797	Sequencing	Read depth and paired-end mapping	Heterozygous	2,871
essv14047539	copy number loss	SAMN01761245	Sequencing	Read depth and paired-end mapping	Heterozygous	3,282
essv14047540	copy number loss	SAMN01036810	Sequencing	Read depth and paired-end mapping	Heterozygous	3,221
essv14047541	copy number loss	SAMN01090886	Sequencing	Read depth and paired-end mapping	Heterozygous	3,245
essv14047542	copy number loss	SAMN01761319	Sequencing	Read depth and paired-end mapping	Heterozygous	3,229
essv14047543	copy number loss	SAMN01761335	Sequencing	Read depth and paired-end mapping	Heterozygous	2,544
essv14047544	copy number loss	SAMN01090786	Sequencing	Read depth and paired-end mapping	Homozygous	3,121
essv14047545	copy number loss	SAMN01090803	Sequencing	Read depth and paired-end mapping	Heterozygous	3,000
essv14047546	copy number loss	SAMN01090829	Sequencing	Read depth and paired-end mapping	Heterozygous	2,716
essv14047547	copy number loss	SAMN00001040	Sequencing	Read depth and paired-end mapping	Heterozygous	3,220
essv14047548	copy number loss	SAMN00000551	Sequencing	Read depth and paired-end mapping	Heterozygous	2,913
essv14047549	copy number loss	SAMN00001677	Sequencing	Read depth and paired-end mapping	Heterozygous	2,665
essv14047550	copy number loss	SAMN00001680	Sequencing	Read depth and paired-end mapping	Heterozygous	2,502
essv14047551	copy number loss	SAMN00001690	Sequencing	Read depth and paired-end mapping	Heterozygous	2,543
essv14047552	copy number loss	SAMN00001691	Sequencing	Read depth and paired-end mapping	Heterozygous	2,479
essv14047553	copy number loss	SAMN00000569	Sequencing	Read depth and paired-end mapping	Heterozygous	2,809
essv14047554	copy number loss	SAMN00001693	Sequencing	Read depth and paired-end mapping	Heterozygous	3,331
essv14047555	copy number loss	SAMN00000571	Sequencing	Read depth and paired-end mapping	Heterozygous	3,230
essv14047556	copy number loss	SAMN00001695	Sequencing	Read depth and paired-end mapping	Heterozygous	2,582
essv14047557	copy number loss	SAMN00001097	Sequencing	Read depth and paired-end mapping	Heterozygous	2,969
essv14047558	copy number loss	SAMN00001102	Sequencing	Read depth and paired-end mapping	Heterozygous	2,846
essv14047559	copy number loss	SAMN00001121	Sequencing	Read depth and paired-end mapping	Heterozygous	3,030
essv14047560	copy number loss	SAMN00001127	Sequencing	Read depth and paired-end mapping	Heterozygous	3,174
essv14047561	copy number loss	SAMN00001133	Sequencing	Read depth and paired-end mapping	Heterozygous	3,069
essv14047562	copy number loss	SAMN00001136	Sequencing	Read depth and paired-end mapping	Heterozygous	3,055
essv14047563	copy number loss	SAMN00001146	Sequencing	Read depth and paired-end mapping	Heterozygous	3,120
essv14047564	copy number loss	SAMN00001150	Sequencing	Read depth and paired-end mapping	Heterozygous	3,142
essv14047565	copy number loss	SAMN00001162	Sequencing	Read depth and paired-end mapping	Heterozygous	2,775
essv14047566	copy number loss	SAMN00001165	Sequencing	Read depth and paired-end mapping	Heterozygous	3,272
essv14047567	copy number loss	SAMN00001179	Sequencing	Read depth and paired-end mapping	Heterozygous	3,049
essv14047568	copy number loss	SAMN00001192	Sequencing	Read depth and paired-end mapping	Heterozygous	3,071
essv14047569	copy number gain	SAMN00263051	Sequencing	Read depth and paired-end mapping	Heterozygous	2,849

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv14047514	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047515	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047516	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047517	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047518	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047519	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047520	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047521	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047522	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047523	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047524	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047525	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047526	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047527	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047528	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047529	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047530	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047531	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047532	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047533	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047534	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047535	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047536	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047537	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047538	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047539	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047540	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047541	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047542	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047543	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047544	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047545	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047546	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047547	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047548	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047549	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047550	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047551	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047552	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047553	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047554	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047555	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047556	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047557	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047558	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047559	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047560	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047561	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047562	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047563	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047564	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047565	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047566	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047567	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047568	Remapped	Perfect	NC_000011.10:g.211 65387_21195613del	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047569	Remapped	Perfect	NC_000011.10:g.211 65387_21195613dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	21,165,387	21,195,613
essv14047514	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047515	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047516	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047517	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047518	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047519	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047520	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047521	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047522	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047523	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047524	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047525	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047526	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047527	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047528	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047529	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047530	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047531	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047532	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047533	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047534	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047535	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047536	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047537	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047538	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047539	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047540	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047541	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047542	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047543	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047544	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047545	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047546	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047547	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047548	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047549	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047550	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047551	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047552	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047553	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047554	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047555	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047556	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159
essv14047557	Submitted genomic		NC_000011.9:g.2118 6933_21217159del	GRCh37 (hg19)		NC_000011.9	Chr11	21,186,933	21,217,159

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dbVar

Database of genomic structural variation

esv3625569

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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.