A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116889



Internal ID21300155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:97699832..97704057hg38UCSC Ensembl
Innerchr1:98165388..98169613hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg384226
hg194226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084977
Samplessample210
Known GenesDPYD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116889
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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