A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659909



Internal ID15396561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76535987..76545843hg38UCSC Ensembl
Innerchr9:79150903..79160759hg19UCSC Ensembl
Innerchr9:78340723..78350579hg18UCSC Ensembl
Innerchr9:76380457..76390313hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389857
hg199857
hg189857
hg179857
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517178
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659909
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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