A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615861



Internal ID16403270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135258742..135419084hg38UCSC Ensembl
Innerchr9:138150588..138310930hg19UCSC Ensembl
Innerchr9:137290409..137450751hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38160343
hg19160343
hg18160343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12979n54
Supporting Variantsnssv1176391
Samples1780854017_A
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615861
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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