A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581880



Internal ID16369289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51416047..51440601hg38UCSC Ensembl
Innerchr2:51643185..51667739hg19UCSC Ensembl
Innerchr2:51496689..51521243hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3824555
hg1924555
hg1824555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6868n54
Supporting Variantsnssv908404
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581880
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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