A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696459



Internal ID15433111
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518992
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696459
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer