A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096927



Internal ID21291390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31065273..31087764hg38UCSC Ensembl
Innerchr5:31065380..31087871hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3822492
hg1922492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115288
Supporting Variants
Samplessample73
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096927
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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