A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615198



Internal ID16055921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112634926..112826971hg38UCSC Ensembl
Innerchr9:115397206..115589251hg19UCSC Ensembl
Innerchr9:114437027..114629072hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38192046
hg19192046
hg18192046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176122
SamplesHGDP00921
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615198
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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