esv2678954

Organism: Homo sapiens

Study:estd199 (1000 Genomes Consortium Phase 1)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:43
Validation:Yes
Clinical Assertions: No
Region Size:13,858

Description:High quality site
Publication(s):1000 Genomes Project Consortium et al. 2012

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: 201 SVs from 54 studies. See in: genome view

Remapped(Score: Perfect):56,573,699-56,587,556

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv2678954	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
esv2678954	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	56,607,727	56,621,584

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv5409334	deletion	SAMN00009153	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,539
essv5412763	deletion	SAMN00006474	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,703
essv5462197	deletion	SAMN00006562	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,667
essv5479686	deletion	SAMN00007729	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,132
essv5519388	deletion	SAMN00007716	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,441
essv5542390	deletion	SAMN00000460	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,651
essv5561886	deletion	SAMN00007792	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,081
essv5579438	deletion	SAMN00001619	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,363
essv5592983	deletion	SAMN00004689	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,655
essv5628611	deletion	SAMN00000439	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,142
essv5634865	deletion	SAMN00001609	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,305
essv5643443	deletion	SAMN00009093	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,449
essv5652943	deletion	SAMN00007752	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,122
essv5674688	deletion	SAMN00000926	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,337
essv5714503	deletion	SAMN00007785	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,287
essv5746202	deletion	SAMN00000435	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,556
essv5746339	deletion	SAMN00000422	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,640
essv5753832	deletion	SAMN00000429	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,527
essv5762137	deletion	SAMN00000418	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,714
essv5764075	deletion	SAMN00006394	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,648
essv5764277	deletion	SAMN00000538	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	933
essv5792338	deletion	SAMN00000424	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,563
essv5862938	deletion	SAMN00001611	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,237
essv5865872	deletion	SAMN00000514	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,014
essv5883361	deletion	SAMN00006372	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,554
essv5887314	deletion	SAMN00006513	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,611
essv5963988	deletion	SAMN00001649	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,053
essv6045077	deletion	SAMN00006501	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,714
essv6071047	deletion	SAMN00006571	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,708
essv6074754	deletion	SAMN00014342	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,537
essv6139401	deletion	SAMN00006486	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,453
essv6159476	deletion	SAMN00006561	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,714
essv6191824	deletion	SAMN00000523	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,001
essv6210678	deletion	SAMN00006505	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,623
essv6292042	deletion	SAMN00000506	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,170
essv6295242	deletion	SAMN00000534	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,195
essv6330828	deletion	SAMN00000524	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,146
essv6344524	deletion	SAMN00000922	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,153
essv6438543	deletion	SAMN00006508	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,015
essv6465459	deletion	SAMN00000428	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,733
essv6492499	deletion	SAMN00006454	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,600
essv6534912	deletion	SAMN00006522	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,660
essv6567069	deletion	SAMN00006460	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,601

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv5409334	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5412763	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5462197	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5479686	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5519388	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5542390	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5561886	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5579438	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5592983	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5628611	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5634865	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5643443	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5652943	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5674688	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5714503	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5746202	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5746339	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5753832	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5762137	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5764075	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5764277	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5792338	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5862938	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5865872	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5883361	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5887314	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5963988	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6045077	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6071047	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6074754	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6139401	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6159476	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6191824	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6210678	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6292042	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6295242	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6330828	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6344524	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6438543	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6465459	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6492499	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6534912	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv6567069	Remapped	Perfect	NC_000003.12:g.565 73699_56587556delG	GRCh38.p12	First Pass	NC_000003.12	Chr3	56,573,699	56,587,556
essv5409334	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5412763	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5462197	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5479686	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5519388	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5542390	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5561886	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5579438	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5592983	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5628611	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5634865	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5643443	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5652943	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5674688	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5714503	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5746202	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5746339	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5753832	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5762137	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5764075	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5764277	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5792338	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5862938	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5865872	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5883361	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5887314	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv5963988	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6045077	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6071047	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6074754	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6139401	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6159476	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6191824	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6210678	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6292042	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6295242	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6330828	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6344524	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6438543	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6465459	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6492499	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6534912	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584
essv6567069	Submitted genomic		NC_000003.11:g.566 07727_56621584delG	GRCh37 (hg19)		NC_000003.11	Chr3	56,607,727	56,621,584

Validation Information

Variant Call ID	Experiment ID	Sample ID	Method	Analysis	Result
essv5762137	7	SAMN00000418	SNP array	Probe signal intensity	Pass
essv5746339	7	SAMN00000422	SNP array	Probe signal intensity	Pass
essv5792338	7	SAMN00000424	SNP array	Probe signal intensity	Pass
essv6465459	7	SAMN00000428	SNP array	Probe signal intensity	Pass
essv5753832	7	SAMN00000429	SNP array	Probe signal intensity	Pass
essv5746202	7	SAMN00000435	SNP array	Probe signal intensity	Pass
essv5628611	7	SAMN00000439	SNP array	Probe signal intensity	Pass
essv5542390	7	SAMN00000460	SNP array	Probe signal intensity	Pass
essv6292042	7	SAMN00000506	SNP array	Probe signal intensity	Pass
essv5865872	7	SAMN00000514	SNP array	Probe signal intensity	Pass
essv6191824	7	SAMN00000523	SNP array	Probe signal intensity	Pass
essv6330828	7	SAMN00000524	SNP array	Probe signal intensity	Pass
essv6295242	7	SAMN00000534	SNP array	Probe signal intensity	Pass
essv5764277	7	SAMN00000538	SNP array	Probe signal intensity	Pass
essv6344524	7	SAMN00000922	SNP array	Probe signal intensity	Pass
essv5674688	7	SAMN00000926	SNP array	Probe signal intensity	Pass
essv5634865	7	SAMN00001609	SNP array	Probe signal intensity	Pass
essv5862938	7	SAMN00001611	SNP array	Probe signal intensity	Pass
essv5579438	7	SAMN00001619	SNP array	Probe signal intensity	Pass
essv5963988	7	SAMN00001649	SNP array	Probe signal intensity	Pass
essv5592983	7	SAMN00004689	SNP array	Probe signal intensity	Pass
essv5883361	7	SAMN00006372	SNP array	Probe signal intensity	Pass
essv5764075	7	SAMN00006394	SNP array	Probe signal intensity	Pass
essv6492499	7	SAMN00006454	SNP array	Probe signal intensity	Pass
essv6567069	7	SAMN00006460	SNP array	Probe signal intensity	Pass
essv5412763	7	SAMN00006474	SNP array	Probe signal intensity	Pass
essv6139401	7	SAMN00006486	SNP array	Probe signal intensity	Pass
essv6045077	7	SAMN00006501	SNP array	Probe signal intensity	Pass
essv6210678	7	SAMN00006505	SNP array	Probe signal intensity	Pass
essv6438543	7	SAMN00006508	SNP array	Probe signal intensity	Pass
essv5887314	7	SAMN00006513	SNP array	Probe signal intensity	Pass
essv6534912	7	SAMN00006522	SNP array	Probe signal intensity	Pass
essv6159476	7	SAMN00006561	SNP array	Probe signal intensity	Pass
essv5462197	7	SAMN00006562	SNP array	Probe signal intensity	Pass
essv6071047	7	SAMN00006571	SNP array	Probe signal intensity	Pass
essv5519388	7	SAMN00007716	SNP array	Probe signal intensity	Pass
essv5479686	7	SAMN00007729	SNP array	Probe signal intensity	Pass
essv5652943	7	SAMN00007752	SNP array	Probe signal intensity	Pass
essv5714503	7	SAMN00007785	SNP array	Probe signal intensity	Pass
essv5561886	7	SAMN00007792	SNP array	Probe signal intensity	Pass
essv5643443	7	SAMN00009093	SNP array	Probe signal intensity	Pass
essv5409334	7	SAMN00009153	SNP array	Probe signal intensity	Pass
essv6074754	7	SAMN00014342	SNP array	Probe signal intensity	Pass

dbVar

Database of genomic structural variation

esv2678954

Links to Other Resources

Genome View

Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

Validation Information

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant