A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108995



Internal ID21274577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:123510854..123513616hg38UCSC Ensembl
Innerchr5:122846548..122849310hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg382763
hg192763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110277
Supporting Variants
Samplessample208
Known GenesCSNK1G3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108995
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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