A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527201



Internal ID15454494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:148396337..148476698hg38UCSC Ensembl
Innerchr3:148114124..148194485hg19UCSC Ensembl
Innerchr3:149596814..149677175hg18UCSC Ensembl
Innerchr3:149596822..149677183hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3880362
hg1980362
hg1880362
hg1780362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703601
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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