A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664354



Internal ID9930459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43599977..43600158hg38UCSC Ensembl
chr10:44095425..44095606hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6449161, essv5874047, essv6184567, essv5855740, essv6324938, essv5790754, essv5863490, essv5584309, essv6214683, essv5434197, essv6396252, essv5613833, essv6561816, essv6335069, essv6349889, essv6357037, essv6013563, essv5631408, essv5941058, essv6247414, essv6504165, essv5811943, essv6130471, essv5997612, essv5844124, essv5956377, essv5924660, essv6293443, essv5550919, essv5508079, essv6108436, essv5683398
SamplesNA20588, NA12717, NA19703, NA18599, HG01389, HG00318, HG00150, HG01051, HG00271, HG00127, NA11992, NA07347, HG01365, NA20759, HG00236, NA19917, HG00264, HG00320, HG00284, HG00273, HG00331, HG00246, NA20765, NA20801, NA19473, NA20815, NA19773, NA12347, NA19398, NA19713, NA20826, NA20528
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664354
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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