A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518204



Internal ID15098811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131448341..131944854hg38UCSC Ensembl
Innerchr10:133246604..133758358hg19UCSC Ensembl
Innerchr10:133136594..133608348hg18UCSC Ensembl
Innerchr10:133136594..133608348hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38496514
hg19511755
hg18471755
hg17471755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695628
Samples
Known GenesFLJ46300, PPP2R2D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518204
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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