A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661477



Internal ID9927582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73402731..73412724hg38UCSC Ensembl
chr9:76017647..76027640hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389994
hg199994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6541143, essv5491393, essv6185405, essv6250331, essv6004710, essv6395963, essv6194413, essv6388110, essv5691517, essv5813434, essv5623705, essv6326779, essv6236858, essv5884677, essv6125706, essv6272220, essv6255953, essv5896559, essv5823281, essv5517832, essv6011268, essv5571413
SamplesNA20588, NA12717, HG00231, NA11933, HG01389, NA20813, NA20512, NA12751, NA12400, HG00327, HG00270, HG01133, HG00326, HG00178, HG01353, NA12829, NA12249, HG01101, NA19625, HG00336, HG00319, NA20803
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661477
Frequency
Sample Size1151
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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