A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110768



Internal ID21294034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103332659..103337940hg38UCSC Ensembl
Innerchr14:103798996..103804277hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg385282
hg195282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095115
Samplessample359
Known GenesEIF5, SNORA28
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110768
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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