A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666879



Internal ID9932984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180165491..180165641hg38UCSC Ensembl
chr3:179883279..179883429hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5527186, essv6158648, essv5727852, essv6540763, essv5628357, essv5492387, essv5944635, essv5906846, essv6353987, essv5992278, essv5853270, essv5424199, essv5607889, essv5578677, essv6148886, essv5900477, essv6064961, essv5507047, essv5454648, essv5782882, essv6419790, essv5678523, essv5733844, essv5627370, essv5609861, essv6293932, essv5502682, essv5840296, essv5697344
SamplesNA19394, NA18502, NA19703, NA18924, NA20294, NA19107, NA19381, NA19379, NA19382, NA19198, NA19313, NA19239, NA19247, NA19403, NA19347, HG01390, NA19449, NA12892, HG01497, NA19240, NA19334, NA19428, NA19467, NA19818, NA20348, NA18873, NA18488, NA19429, HG00553
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666879
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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