A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110208



Internal ID21293474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20707297..20710749hg38UCSC Ensembl
Innerchr14:21175456..21178908hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383453
hg193453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv319n145
Supporting Variantsnssv14095313, nssv14093989
Samplessample299, sample124
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110208
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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