A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674872



Internal ID9940977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36987790..36987896hg38UCSC Ensembl
Outerchr6:36987419..36988266hg38UCSC Ensembl
Innerchr6:36955566..36955672hg19UCSC Ensembl
Outerchr6:36955195..36956042hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6574248, essv6175186, essv5623638, essv5564773, essv6259809, essv5530447, essv6086737, essv5627825, essv5861881, essv6388359, essv5667654, essv5763084, essv6245823, essv6217972, essv5584508, essv5498450, essv5483739, essv6311311, essv6427972, essv6315986, essv5698330, essv5469087, essv6120381, essv5749817, essv6505514, essv5644562, essv5702421, essv6218766, essv6009056, essv6447354, essv6504396, essv5698226, essv6469147, essv5398473, essv5721905, essv5524876, essv5425037, essv6500896, essv5457863, essv5477498, essv6124157, essv6523950, essv6232043, essv5535850, essv6594492
SamplesHG01060, HG01173, HG01052, HG01079, HG01188, HG01066, HG00737, HG01051, HG00641, HG01070, HG01168, HG00736, HG01083, HG01069, HG01080, HG01067, HG01170, HG01072, HG01176, HG01198, HG01048, HG01183, HG01187, HG01171, HG00732, HG01095, HG00740, HG01047, HG01102, HG01073, HG01197, HG01182, HG01101, HG01107, HG01075, HG01190, HG00734, HG00638, HG01174, HG01108, HG01055, HG01082, HG01191, HG01061, HG00553
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674872
Frequency
Sample Size1151
Observed Gain0
Observed Loss45
Observed Complex0
Frequencyn/a


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