A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176389



Internal ID15854272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135400692hg38UCSC Ensembl
Innerchr9:138149166..138292538hg19UCSC Ensembl
Innerchr9:137288987..137432359hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38143373
hg19143373
hg18143373
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615851
Supporting Variants
Samples1780862066_A
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176389
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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