A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528281



Internal ID8422556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:132650771..132682252hg38UCSC Ensembl
Innerchr5:131986463..132017944hg19UCSC Ensembl
Innerchr5:132014362..132045843hg18UCSC Ensembl
Innerchr5:132014362..132045843hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3831482
hg1931482
hg1831482
hg1731482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704851
Samples
Known GenesIL13, IL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528281
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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