A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518992



Internal ID15446285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111049165..111149333hg38UCSC Ensembl
Innerchr9:113811445..113911613hg19UCSC Ensembl
Innerchr9:112851266..112951434hg18UCSC Ensembl
Innerchr9:110891000..110991168hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38100169
hg19100169
hg18100169
hg17100169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696459
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518992
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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