A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114216



Internal ID21297482
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 StatusM
Merged Variantsdgv978n145
Supporting Variantsnssv14109289
Samplessample299
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114216
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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