A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581009



Internal ID16368418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062091..13138533hg38UCSC Ensembl
Innerchr2:13202216..13278658hg19UCSC Ensembl
Innerchr2:13119667..13196109hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3876443
hg1976443
hg1876443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6700n54
Supporting Variantsnssv903808, nssv903809
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581009
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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