esv2675076

Organism: Homo sapiens

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

Variant Calls:33
Validation:Yes
Clinical Assertions: No
Region Size:10,348

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: 600 SVs from 77 studies. See in: genome view

Remapped(Score: Perfect):99,874,440-99,884,787

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
esv2675076	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
esv2675076	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv5430188	deletion	SAMN00007708	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,132
essv5438625	deletion	SAMN00009192	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,161
essv5564475	deletion	SAMN00007705	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,063
essv5742694	deletion	SAMN00009117	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,813
essv5824597	deletion	SAMN00009125	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,711
essv5847095	deletion	SAMN00009171	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,640
essv5861652	deletion	SAMN00009130	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,791
essv5907214	deletion	SAMN00007780	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	744
essv6034207	deletion	SAMN00007707	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,115
essv6091770	deletion	SAMN00009172	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,731
essv6100841	deletion	SAMN00007722	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,201
essv6112366	deletion	SAMN00006583	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,292
essv6133034	deletion	SAMN00007747	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,108
essv6153001	deletion	SAMN00009193	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,085
essv6165754	deletion	SAMN00007783	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	817
essv6200613	deletion	SAMN00009128	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,219
essv6204023	deletion	SAMN00009120	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,658
essv6265950	deletion	SAMN00006579	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,224
essv6322802	deletion	SAMN00006596	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,607
essv6323062	deletion	SAMN00007786	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,118
essv6339139	deletion	SAMN00007726	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,102
essv6346869	deletion	SAMN00009184	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,318
essv6351622	deletion	SAMN00007776	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	831
essv6397711	deletion	SAMN00007732	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,164
essv6414956	deletion	SAMN00006589	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,904
essv6470008	deletion	SAMN00007759	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	815
essv6475925	deletion	SAMN00007779	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	853
essv6486184	deletion	SAMN00009116	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,780
essv6520553	deletion	SAMN00006538	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,111
essv6531622	deletion	SAMN00009187	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,487
essv6533136	deletion	SAMN00009168	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	752
essv6584774	deletion	SAMN00009126	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,897
essv6592905	deletion	SAMN00007791	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,181

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
essv5430188	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv5438625	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv5564475	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv5742694	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv5824597	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv5847095	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv5861652	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv5907214	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6034207	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6091770	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6100841	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6112366	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6133034	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6153001	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6165754	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6200613	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6204023	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6265950	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6322802	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6323062	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6339139	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6346869	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6351622	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6397711	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6414956	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6470008	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6475925	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6486184	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6520553	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6531622	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6533136	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6584774	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv6592905	Remapped	Perfect	NC_000015.10:g.(99 874440_99874811)_( 99884317_99884787) del	GRCh38.p12	First Pass	NC_000015.10	Chr15	99,874,440	99,874,811	99,884,317	99,884,787
essv5430188	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv5438625	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv5564475	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv5742694	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv5824597	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv5847095	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv5861652	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv5907214	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6034207	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6091770	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6100841	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6112366	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6133034	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6153001	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6165754	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6200613	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6204023	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6265950	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6322802	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6323062	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6339139	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6346869	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6351622	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6397711	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6414956	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6470008	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6475925	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6486184	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6520553	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6531622	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6533136	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6584774	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992
essv6592905	Submitted genomic		NC_000015.9:g.(100 414645_100415016)_ (100424522_1004249 92)del	GRCh37 (hg19)		NC_000015.9	Chr15	100,414,645	100,415,016	100,424,522	100,424,992

Validation Information

Variant Call ID	Experiment ID	Sample ID	Method	Analysis	Result
essv6520553	7	SAMN00006538	SNP array	Probe signal intensity	Pass
essv6265950	7	SAMN00006579	SNP array	Probe signal intensity	Pass
essv6112366	7	SAMN00006583	SNP array	Probe signal intensity	Pass
essv6414956	7	SAMN00006589	SNP array	Probe signal intensity	Pass
essv6322802	7	SAMN00006596	SNP array	Probe signal intensity	Pass
essv5564475	7	SAMN00007705	SNP array	Probe signal intensity	Pass
essv6034207	7	SAMN00007707	SNP array	Probe signal intensity	Pass
essv5430188	7	SAMN00007708	SNP array	Probe signal intensity	Pass
essv6100841	7	SAMN00007722	SNP array	Probe signal intensity	Pass
essv6339139	7	SAMN00007726	SNP array	Probe signal intensity	Pass
essv6397711	7	SAMN00007732	SNP array	Probe signal intensity	Pass
essv6133034	7	SAMN00007747	SNP array	Probe signal intensity	Pass
essv6470008	7	SAMN00007759	SNP array	Probe signal intensity	Pass
essv6351622	7	SAMN00007776	SNP array	Probe signal intensity	Pass
essv6475925	7	SAMN00007779	SNP array	Probe signal intensity	Pass
essv5907214	7	SAMN00007780	SNP array	Probe signal intensity	Pass
essv6165754	7	SAMN00007783	SNP array	Probe signal intensity	Pass
essv6323062	7	SAMN00007786	SNP array	Probe signal intensity	Pass
essv6592905	7	SAMN00007791	SNP array	Probe signal intensity	Pass
essv6486184	7	SAMN00009116	SNP array	Probe signal intensity	Pass
essv5742694	7	SAMN00009117	SNP array	Probe signal intensity	Pass
essv6204023	7	SAMN00009120	SNP array	Probe signal intensity	Pass
essv5824597	7	SAMN00009125	SNP array	Probe signal intensity	Pass
essv6584774	7	SAMN00009126	SNP array	Probe signal intensity	Pass
essv6200613	7	SAMN00009128	SNP array	Probe signal intensity	Pass
essv5861652	7	SAMN00009130	SNP array	Probe signal intensity	Pass
essv6533136	7	SAMN00009168	SNP array	Probe signal intensity	Pass
essv5847095	7	SAMN00009171	SNP array	Probe signal intensity	Pass
essv6091770	7	SAMN00009172	SNP array	Probe signal intensity	Pass
essv6346869	7	SAMN00009184	SNP array	Probe signal intensity	Pass
essv6531622	7	SAMN00009187	SNP array	Probe signal intensity	Pass
essv5438625	7	SAMN00009192	SNP array	Probe signal intensity	Pass
essv6153001	7	SAMN00009193	SNP array	Probe signal intensity	Pass

dbVar

Database of genomic structural variation

esv2675076

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