A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681068



Internal ID15417720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135414214hg38UCSC Ensembl
Innerchr9:138149166..138306060hg19UCSC Ensembl
Innerchr9:137288987..137445881hg18UCSC Ensembl
Innerchr9:135375111..135532005hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38156895
hg19156895
hg18156895
hg17156895
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)nssv681068
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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