A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528583



Internal ID15455876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:89606728..89607008hg38UCSC Ensembl
Innerchr5:88902545..88902825hg19UCSC Ensembl
Innerchr5:88938301..88938581hg18UCSC Ensembl
Innerchr5:88938301..88938581hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38281
hg19281
hg18281
hg17281
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705204
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528583
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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