A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697974



Internal ID15087940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77195973..77387544hg38UCSC Ensembl
Innerchr9:79810889..80002460hg19UCSC Ensembl
Innerchr9:79000709..79192280hg18UCSC Ensembl
Innerchr9:77040443..77232014hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38191572
hg19191572
hg18191572
hg17191572
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521364
Supporting Variants
Samples
Known GenesVPS13A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697974
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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