A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665506



Internal ID9584925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13831302..13831408hg38UCSC Ensembl
Outerchr19:13830931..13831778hg38UCSC Ensembl
Innerchr19:13942116..13942222hg19UCSC Ensembl
Outerchr19:13941745..13942592hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6143623, essv6305111, essv6554284, essv5518865, essv5552302, essv5643663, essv5992829, essv6058329, essv5989351, essv5399181, essv6447530, essv6423668, essv5890167, essv6016983, essv6123436, essv6462166, essv6457803, essv6289303, essv6201357, essv6387830, essv6518991, essv5685392, essv5831397, essv6529660, essv5671284, essv5964959, essv5433041, essv6165651, essv6449298, essv5451423, essv5474591, essv5908180, essv6234267, essv5763527, essv5942540, essv6167180, essv6385936, essv6315454, essv6383223, essv5430592, essv5590656, essv6578905, essv6500188, essv6520927, essv5408113, essv6236340, essv5965001, essv5783549, essv5471930, essv5851907
SamplesHG00734, HG01072, HG01052, HG01075, HG01055, HG01173, HG01083, HG00731, HG01098, HG01079, HG01197, HG01051, HG01082, HG01174, HG00553, HG01182, HG01167, HG01188, HG01204, HG01101, HG01168, HG00737, HG01171, HG00554, HG01107, HG01048, HG01061, HG01183, HG01047, HG01187, HG01097, HG01191, HG00640, HG01066, HG00732, HG01073, HG01170, HG01069, HG01176, HG01080, HG00740, HG01070, HG01060, HG01190, HG01095, HG01108, HG00641, HG01102, HG01067, HG01198
Known GenesZSWIM4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665506
Frequency
Sample Size1151
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


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