A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521488



Internal ID15448781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20631634..20649912hg38UCSC Ensembl
Innerchr9:20631633..20649911hg19UCSC Ensembl
Innerchr9:20621633..20639911hg18UCSC Ensembl
Innerchr9:20621633..20639911hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3818279
hg1918279
hg1818279
hg1718279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698099
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521488
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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