A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095553



Internal ID21275002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89435050..89471609hg38UCSC Ensembl
Innerchr14:89901394..89937953hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3836560
hg1936560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111206
Supporting Variants
Samplessample216
Known GenesFOXN3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095553
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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