A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110495



Internal ID21293761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99479283..99483104hg38UCSC Ensembl
Innerchr14:99945620..99949441hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383822
hg193822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095537
Samplessample208
Known GenesCCNK, SETD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110495
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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