A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659679



Internal ID15049645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29920842..29923365hg38UCSC Ensembl
Innerchr9:29920840..29923363hg19UCSC Ensembl
Innerchr9:29910840..29913363hg18UCSC Ensembl
Innerchr9:29910840..29913363hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg382524
hg192524
hg182524
hg172524
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659679
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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