A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674923



Internal ID15064889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66982077..67162484hg38UCSC Ensembl
Innerchr10:68741835..68922242hg19UCSC Ensembl
Innerchr10:68411841..68592248hg18UCSC Ensembl
Innerchr10:68411841..68592248hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38180408
hg19180408
hg18180408
hg17180408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520745
Supporting Variants
Samples
Known GenesCTNNA3, LRRTM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674923
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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