esv2672784

Organism: Homo sapiens

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

Variant Calls:31
Validation:Yes
Clinical Assertions: No
Region Size:11,748

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: 933 SVs from 79 studies. See in: genome view

Remapped(Score: Perfect):78,337,648-78,349,395

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
esv2672784	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
esv2672784	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv5426824	deletion	SAMN00001107	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	943
essv5442574	deletion	SAMN00001190	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,291
essv5443514	deletion	SAMN00001149	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,599
essv5444874	deletion	SAMN00001111	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	811
essv5473184	deletion	SAMN00001174	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,500
essv5483122	deletion	SAMN00001134	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,508
essv5516191	deletion	SAMN00001148	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,511
essv5529905	deletion	SAMN00001120	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,364
essv5533839	deletion	SAMN00001175	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,327
essv5573754	deletion	SAMN00001189	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,771
essv5607522	deletion	SAMN00001186	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,212
essv5739573	deletion	SAMN00001193	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,179
essv5771995	deletion	SAMN00001132	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,614
essv5795536	deletion	SAMN00001131	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,611
essv5920646	deletion	SAMN00001188	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,129
essv5955667	deletion	SAMN00001158	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,358
essv6034335	deletion	SAMN00001152	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,509
essv6081222	deletion	SAMN00001150	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,706
essv6097103	deletion	SAMN00001138	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,561
essv6140620	deletion	SAMN00001139	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,535
essv6168322	deletion	SAMN00001159	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,248
essv6277782	deletion	SAMN00001137	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,647
essv6293725	deletion	SAMN00001106	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	953
essv6299648	deletion	SAMN00001130	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,544
essv6303105	deletion	SAMN00001192	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,334
essv6373505	deletion	SAMN00001164	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,515
essv6403339	deletion	SAMN00001125	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,568
essv6408399	deletion	SAMN00001166	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,284
essv6555798	deletion	SAMN00001191	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,461
essv6575050	deletion	SAMN00001105	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	859
essv6590154	deletion	SAMN00001102	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,259

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
essv5426824	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5442574	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5443514	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5444874	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5473184	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5483122	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5516191	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5529905	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5533839	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5573754	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5607522	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5739573	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5771995	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5795536	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5920646	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5955667	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6034335	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6081222	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6097103	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6140620	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6168322	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6277782	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6293725	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6299648	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6303105	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6373505	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6403339	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6408399	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6555798	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6575050	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv6590154	Remapped	Perfect	NC_000016.10:g.(78 337648_78338019)_( 78349025_78349395) del	GRCh38.p12	First Pass	NC_000016.10	Chr16	78,337,648	78,338,019	78,349,025	78,349,395
essv5426824	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5442574	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5443514	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5444874	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5473184	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5483122	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5516191	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5529905	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5533839	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5573754	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5607522	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5739573	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5771995	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5795536	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5920646	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv5955667	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6034335	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6081222	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6097103	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6140620	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6168322	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6277782	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6293725	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6299648	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6303105	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6373505	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6403339	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6408399	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6555798	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6575050	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292
essv6590154	Submitted genomic		NC_000016.9:g.(783 71545_78371916)_(7 8382922_78383292)d el	GRCh37 (hg19)		NC_000016.9	Chr16	78,371,545	78,371,916	78,382,922	78,383,292

Validation Information

Variant Call ID	Experiment ID	Sample ID	Method	Analysis	Result
essv6590154	9	SAMN00001102	Oligo aCGH	Probe signal intensity	Pass
essv6575050	9	SAMN00001105	Oligo aCGH	Probe signal intensity	Pass
essv6293725	9	SAMN00001106	Oligo aCGH	Probe signal intensity	Pass
essv5426824	9	SAMN00001107	Oligo aCGH	Probe signal intensity	Pass
essv5444874	9	SAMN00001111	Oligo aCGH	Probe signal intensity	Pass
essv5529905	9	SAMN00001120	Oligo aCGH	Probe signal intensity	Pass
essv6403339	9	SAMN00001125	Oligo aCGH	Probe signal intensity	Pass
essv6299648	9	SAMN00001130	Oligo aCGH	Probe signal intensity	Pass
essv5795536	9	SAMN00001131	Oligo aCGH	Probe signal intensity	Pass
essv5771995	9	SAMN00001132	Oligo aCGH	Probe signal intensity	Pass
essv5483122	9	SAMN00001134	Oligo aCGH	Probe signal intensity	Pass
essv6277782	9	SAMN00001137	Oligo aCGH	Probe signal intensity	Pass
essv6097103	9	SAMN00001138	Oligo aCGH	Probe signal intensity	Pass
essv6140620	9	SAMN00001139	Oligo aCGH	Probe signal intensity	Pass
essv5516191	9	SAMN00001148	Oligo aCGH	Probe signal intensity	Pass
essv5443514	9	SAMN00001149	Oligo aCGH	Probe signal intensity	Pass
essv6081222	9	SAMN00001150	Oligo aCGH	Probe signal intensity	Pass
essv6034335	9	SAMN00001152	Oligo aCGH	Probe signal intensity	Pass
essv5955667	9	SAMN00001158	Oligo aCGH	Probe signal intensity	Pass
essv6168322	9	SAMN00001159	Oligo aCGH	Probe signal intensity	Pass
essv6373505	9	SAMN00001164	Oligo aCGH	Probe signal intensity	Pass
essv6408399	9	SAMN00001166	Oligo aCGH	Probe signal intensity	Pass
essv5473184	9	SAMN00001174	Oligo aCGH	Probe signal intensity	Pass
essv5533839	9	SAMN00001175	Oligo aCGH	Probe signal intensity	Pass
essv5607522	9	SAMN00001186	Oligo aCGH	Probe signal intensity	Pass
essv5920646	9	SAMN00001188	Oligo aCGH	Probe signal intensity	Pass
essv5573754	9	SAMN00001189	Oligo aCGH	Probe signal intensity	Pass
essv5442574	9	SAMN00001190	Oligo aCGH	Probe signal intensity	Pass
essv6555798	9	SAMN00001191	Oligo aCGH	Probe signal intensity	Pass
essv6303105	9	SAMN00001192	Oligo aCGH	Probe signal intensity	Pass
essv5739573	9	SAMN00001193	Oligo aCGH	Probe signal intensity	Pass
essv6590154	7	SAMN00001102	SNP array	Probe signal intensity	Pass
essv6575050	7	SAMN00001105	SNP array	Probe signal intensity	Pass
essv6293725	7	SAMN00001106	SNP array	Probe signal intensity	Pass
essv5426824	7	SAMN00001107	SNP array	Probe signal intensity	Pass
essv5444874	7	SAMN00001111	SNP array	Probe signal intensity	Pass
essv5529905	7	SAMN00001120	SNP array	Probe signal intensity	Pass
essv6403339	7	SAMN00001125	SNP array	Probe signal intensity	Pass
essv6299648	7	SAMN00001130	SNP array	Probe signal intensity	Pass
essv5795536	7	SAMN00001131	SNP array	Probe signal intensity	Pass
essv5771995	7	SAMN00001132	SNP array	Probe signal intensity	Pass
essv5483122	7	SAMN00001134	SNP array	Probe signal intensity	Pass
essv6277782	7	SAMN00001137	SNP array	Probe signal intensity	Pass
essv6097103	7	SAMN00001138	SNP array	Probe signal intensity	Pass
essv6140620	7	SAMN00001139	SNP array	Probe signal intensity	Pass
essv5516191	7	SAMN00001148	SNP array	Probe signal intensity	Pass
essv5443514	7	SAMN00001149	SNP array	Probe signal intensity	Pass
essv6081222	7	SAMN00001150	SNP array	Probe signal intensity	Pass
essv6034335	7	SAMN00001152	SNP array	Probe signal intensity	Pass
essv5955667	7	SAMN00001158	SNP array	Probe signal intensity	Pass
essv6168322	7	SAMN00001159	SNP array	Probe signal intensity	Pass
essv6373505	7	SAMN00001164	SNP array	Probe signal intensity	Pass
essv6408399	7	SAMN00001166	SNP array	Probe signal intensity	Pass
essv5473184	7	SAMN00001174	SNP array	Probe signal intensity	Pass
essv5533839	7	SAMN00001175	SNP array	Probe signal intensity	Pass
essv5607522	7	SAMN00001186	SNP array	Probe signal intensity	Pass
essv5920646	7	SAMN00001188	SNP array	Probe signal intensity	Pass
essv5573754	7	SAMN00001189	SNP array	Probe signal intensity	Pass
essv5442574	7	SAMN00001190	SNP array	Probe signal intensity	Pass
essv6555798	7	SAMN00001191	SNP array	Probe signal intensity	Pass
essv6303105	7	SAMN00001192	SNP array	Probe signal intensity	Pass
essv5739573	7	SAMN00001193	SNP array	Probe signal intensity	Pass

dbVar

Database of genomic structural variation

esv2672784

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