A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562374



Internal ID16349783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77373072..77513130hg38UCSC Ensembl
Innerchr13:77947207..78087265hg19UCSC Ensembl
Innerchr13:76845208..76985266hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38140059
hg19140059
hg18140059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815800
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562374
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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