A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518079



Internal ID15445372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33872548..33884633hg38UCSC Ensembl
Innerchr3:33914040..33926125hg19UCSC Ensembl
Innerchr3:33889044..33901129hg18UCSC Ensembl
Innerchr3:33889044..33901129hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3812086
hg1912086
hg1812086
hg1712086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695492
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518079
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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