A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114545



Internal ID21297811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93182260..93188991hg38UCSC Ensembl
Innerchr14:93648605..93655336hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386732
hg196732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096316
Samplessample275
Known GenesMOAP1, TMEM251
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114545
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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