A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115880



Internal ID21299146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20707297..20710643hg38UCSC Ensembl
Innerchr14:21175456..21178802hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383347
hg193347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv319n145
Supporting Variantsnssv14094098, nssv14095376, nssv14095185
Samplessample146, sample44, sample385
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115880
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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