A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529022



Internal ID15456315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:138641163..138656163hg38UCSC Ensembl
Innerchr5:137976852..137991852hg19UCSC Ensembl
Innerchr5:138004751..138019751hg18UCSC Ensembl
Innerchr5:138004751..138019751hg17UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3815001
hg1915001
hg1815001
hg1715001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705733
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529022
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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