A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615613



Internal ID16056336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133161872..133320327hg38UCSC Ensembl
Innerchr9:136037259..136187163hg19UCSC Ensembl
Innerchr9:135027080..135176984hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38158456
hg19149905
hg18149905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12930n54
Supporting Variantsnssv1176518
SamplesHGDP00547
Known GenesABO, GBGT1, OBP2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615613
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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