A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580865



Internal ID16368274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5308496..5360169hg38UCSC Ensembl
Innerchr2:5448629..5500302hg19UCSC Ensembl
Innerchr2:5366080..5417753hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3851674
hg1951674
hg1851674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150707
SamplesHGDP00607
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580865
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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