A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112896



Internal ID21296162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66554953..66614262hg38UCSC Ensembl
Innerchr14:67021671..67080980hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3859310
hg1959310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094000
Samplessample302
Known GenesGPHN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112896
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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