A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097489



Internal ID21268890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163793242..163795758hg38UCSC Ensembl
Innerchr5:163220248..163222764hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382517
hg192517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110260
Supporting Variants
Samplessample131
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097489
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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