A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658114



Internal ID15394766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135420547hg38UCSC Ensembl
Innerchr9:138149166..138312393hg19UCSC Ensembl
Innerchr9:137288987..137452214hg18UCSC Ensembl
Innerchr9:135375111..135538338hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38163228
hg19163228
hg18163228
hg17163228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517428
Supporting Variants
Samples
Known GenesC9orf62
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658114
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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