A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518148



Internal ID15445441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113126328..113127939hg38UCSC Ensembl
Innerchr3:112845175..112846786hg19UCSC Ensembl
Innerchr3:114327865..114329476hg18UCSC Ensembl
Innerchr3:114327865..114329476hg17UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg381612
hg191612
hg181612
hg171612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695569
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518148
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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