A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113975



Internal ID21297241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64463960..64467172hg38UCSC Ensembl
Innerchr14:64930678..64933890hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg383213
hg193213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095094
Samplessample348
Known GenesAKAP5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113975
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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