A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613851



Internal ID16401260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24457293..24495243hg38UCSC Ensembl
Innerchr9:24457291..24495241hg19UCSC Ensembl
Innerchr9:24447291..24485241hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3837951
hg1937951
hg1837951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1131865
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613851
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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