A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523462



Internal ID15450755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39452367..39458669hg38UCSC Ensembl
Innerchr3:39493858..39500160hg19UCSC Ensembl
Innerchr3:39468862..39475164hg18UCSC Ensembl
Innerchr3:39468862..39475164hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386303
hg196303
hg186303
hg176303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699220
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523462
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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