A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581331



Internal ID16368740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33770672..33818359hg38UCSC Ensembl
Innerchr2:33995739..34043426hg19UCSC Ensembl
Innerchr2:33849243..33896930hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3847688
hg1947688
hg1847688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv905026
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581331
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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