A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581332



Internal ID16368741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33818785..33950910hg38UCSC Ensembl
Innerchr2:34043852..34175977hg19UCSC Ensembl
Innerchr2:33897356..34029481hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38132126
hg19132126
hg18132126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6757n54
Supporting Variantsnssv1150206
SamplesHGDP00588
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581332
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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