A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097307



Internal ID21292180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151386886..151412970hg38UCSC Ensembl
Innerchr5:150766447..150792531hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3826085
hg1926085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113438
Supporting Variants
Samplessample84
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097307
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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