A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613709



Internal ID16054432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17899608..17918808hg38UCSC Ensembl
Innerchr9:17899606..17918806hg19UCSC Ensembl
Innerchr9:17889606..17908806hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3819201
hg1919201
hg1819201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129339
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613709
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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