A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520467



Internal ID15101074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33804815..34146647hg38UCSC Ensembl
Innerchr9:33804813..34146645hg19UCSC Ensembl
Innerchr9:33794813..34136645hg18UCSC Ensembl
Innerchr9:33794813..34136645hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38341833
hg19341833
hg18341833
hg17341833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671679, nssv686824
Samples
Known GenesDCAF12, SNORD121A, SNORD121B, UBAP2, UBE2R2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520467
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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