A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661952



Internal ID15398604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112372077..112375196hg38UCSC Ensembl
Innerchr9:115134357..115137476hg19UCSC Ensembl
Innerchr9:114174178..114177297hg18UCSC Ensembl
Innerchr9:112213912..112217031hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383120
hg193120
hg183120
hg173120
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516134
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661952
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