A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656676



Internal ID9922781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152589134..152589370hg38UCSC Ensembl
chr3:152306923..152307159hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5535494, essv6000485, essv6297552, essv6094292, essv5928435, essv5855451, essv5553497, essv6268844, essv6382273, essv6239985, essv6369102, essv6485939, essv5498494, essv6264780, essv5529165, essv5433853, essv5432055, essv5642542, essv5628921, essv5912199, essv6257019, essv5417185, essv5430377, essv5453872, essv5724835, essv6142520, essv6507796, essv5466970, essv6557573, essv6091703, essv6109557, essv5901583
SamplesNA19703, NA19399, NA18561, HG01389, NA20294, NA19355, HG01177, NA19313, NA19384, HG01069, NA19137, NA20342, NA19985, HG01124, NA19437, NA19707, NA19462, NA19391, NA19327, NA19257, NA20296, NA18953, NA18909, NA19380, NA19835, NA19428, NA19376, NA19223, HG00343, HG01377, NA19463, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656676
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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