A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518001



Internal ID15445294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18383382..18408773hg38UCSC Ensembl
Innerchr9:18383380..18408771hg19UCSC Ensembl
Innerchr9:18373380..18398771hg18UCSC Ensembl
Innerchr9:18373380..18398771hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3825392
hg1925392
hg1825392
hg1725392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695413
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518001
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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