A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146801



Internal ID15999987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135422409hg38UCSC Ensembl
Innerchr9:138149166..138314255hg19UCSC Ensembl
Innerchr9:137288987..137454076hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38165090
hg19165090
hg18165090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615857
Supporting Variants
Samples
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1146801
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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