A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581333



Internal ID16368742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33821178..33939119hg38UCSC Ensembl
Innerchr2:34046245..34164186hg19UCSC Ensembl
Innerchr2:33899749..34017690hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38117942
hg19117942
hg18117942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6757n54
Supporting Variantsnssv1150207
SamplesHGDP00578
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581333
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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