A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094064



Internal ID21279877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55183606..55249009hg38UCSC Ensembl
Innerchr14:55650324..55715727hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3865404
hg1965404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114707
Supporting Variants
Samplessample29
Known GenesDLGAP5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094064
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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