A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146799



Internal ID15999985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135418200hg38UCSC Ensembl
Innerchr9:138149166..138310046hg19UCSC Ensembl
Innerchr9:137288987..137449867hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38160881
hg19160881
hg18160881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615855
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)nssv1146799
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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