A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146803



Internal ID15999989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135258742..135406318hg38UCSC Ensembl
Innerchr9:138150588..138298164hg19UCSC Ensembl
Innerchr9:137290409..137437985hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38147577
hg19147577
hg18147577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615859
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)nssv1146803
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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