A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582262



Internal ID16369671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77744657..77799937hg38UCSC Ensembl
Innerchr2:77971783..78027063hg19UCSC Ensembl
Innerchr2:77825291..77880571hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3855281
hg1955281
hg1855281
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6929n54
Supporting Variantsnssv1150237
SamplesHGDP00491
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582262
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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