A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522154



Internal ID15449447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17513285..17740249hg38UCSC Ensembl
Innerchr5:17513394..17740358hg19UCSC Ensembl
Innerchr5:17566394..17776087hg18UCSC Ensembl
Innerchr5:17566394..17776087hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38226965
hg19226965
hg18209694
hg17209694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694927
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522154
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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