A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108789



Internal ID21271191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:67416725..67419619hg38UCSC Ensembl
Innerchr5:66712553..66715447hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg382895
hg192895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114425
Supporting Variants
Samplessample160
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108789
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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