A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516404



Internal ID15097011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:79949017..79949182hg38UCSC Ensembl
Innerchr2:80176143..80176308hg19UCSC Ensembl
Innerchr2:80029654..80029819hg18UCSC Ensembl
Innerchr2:80087801..80087966hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38166
hg19166
hg18166
hg17166
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662297, nssv691986, nssv668105
Samples
Known GenesCTNNA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516404
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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