A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528342



Internal ID15455635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58548399..58557785hg38UCSC Ensembl
Innerchr3:58534126..58543512hg19UCSC Ensembl
Innerchr3:58509166..58518552hg18UCSC Ensembl
Innerchr3:58509166..58518552hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg389387
hg199387
hg189387
hg179387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704924
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528342
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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