A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109289



Internal ID21280429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:65881459..65888683hg38UCSC Ensembl
Innerchr5:65177287..65184511hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg387225
hg197225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114216
Supporting Variants
Samplessample299
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109289
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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