A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671679



Internal ID15061645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33820940..34146647hg38UCSC Ensembl
Innerchr9:33820938..34146645hg19UCSC Ensembl
Innerchr9:33810938..34136645hg18UCSC Ensembl
Innerchr9:33810938..34136645hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38325708
hg19325708
hg18325708
hg17325708
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)nssv671679
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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