A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688920



Internal ID15425572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101882777..102117417hg38UCSC Ensembl
Innerchr9:104645059..104879699hg19UCSC Ensembl
Innerchr9:103684880..103919520hg18UCSC Ensembl
Innerchr9:101724614..101959254hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38234641
hg19234641
hg18234641
hg17234641
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521116
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688920
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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