A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686824



Internal ID15076790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33804815..34127765hg38UCSC Ensembl
Innerchr9:33804813..34127763hg19UCSC Ensembl
Innerchr9:33794813..34117763hg18UCSC Ensembl
Innerchr9:33794813..34117763hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38322951
hg19322951
hg18322951
hg17322951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520467
Supporting Variants
Samples
Known GenesDCAF12, SNORD121A, SNORD121B, UBAP2, UBE2R2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686824
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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