A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615856



Internal ID16403265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135419084hg38UCSC Ensembl
Innerchr9:138149166..138310930hg19UCSC Ensembl
Innerchr9:137288987..137450751hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38161765
hg19161765
hg18161765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12979n54
Supporting Variantsnssv1146800
Samples
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615856
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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