A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626680



Internal ID7013512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65805739..65812837hg38UCSC Ensembl
Innerchr11:65805769..65812808hg38UCSC Ensembl
Outerchr11:65805710..65812867hg38UCSC Ensembl
chr11:65573210..65580308hg19UCSC Ensembl
Innerchr11:65573240..65580279hg19UCSC Ensembl
Outerchr11:65573181..65580338hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387099
hg197099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14191251, essv14191257, essv14191248, essv14191270, essv14191256, essv14191271, essv14191260, essv14191243, essv14191245, essv14191264, essv14191267, essv14191272, essv14191265, essv14191261, essv14191244, essv14191269, essv14191266, essv14191247, essv14191238, essv14191255, essv14191240, essv14191253, essv14191262, essv14191258, essv14191242, essv14191273, essv14191254, essv14191268, essv14191275, essv14191259, essv14191263, essv14191274, essv14191252, essv14191246, essv14191250, essv14191241, essv14191239, essv14191249
SamplesHG03130, HG03298, HG03455, HG03100, HG03139, NA18916, HG02489, NA20278, NA18868, HG02471, NA19189, HG02946, HG01058, NA19027, HG03132, NA19347, HG01095, NA19327, HG02450, HG03428, HG03124, NA19118, NA19042, NA20282, HG03354, NA19095, NA19395, HG02455, NA19835, HG02941, NA19324, HG02580, HG02771, NA20348, HG02971, NA19116, NA19213, HG03162
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626680
Frequency
Sample Size2504
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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