A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613735



Internal ID16401144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19801920..19869440hg38UCSC Ensembl
Innerchr9:19801918..19869438hg19UCSC Ensembl
Innerchr9:19791918..19859438hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3867521
hg1967521
hg1867521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156448
SamplesHGDP00972
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613735
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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