A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520486



Internal ID15447779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58521123..58530656hg38UCSC Ensembl
Innerchr3:58506850..58516383hg19UCSC Ensembl
Innerchr3:58481890..58491423hg18UCSC Ensembl
Innerchr3:58481890..58491423hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg389534
hg199534
hg189534
hg179534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677306, nssv671812
Samples
Known GenesACOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520486
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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