A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581981



Internal ID16369390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52995824..53056196hg38UCSC Ensembl
Innerchr2:53222962..53283334hg19UCSC Ensembl
Innerchr2:53076466..53136838hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3860373
hg1960373
hg1860373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6887n54
Supporting Variantsnssv909353, nssv909352
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581981
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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