A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094201



Internal ID21291918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55127139..55133662hg38UCSC Ensembl
Innerchr14:55593857..55600380hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg386524
hg196524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114036
Supporting Variants
Samplessample81
Known GenesLGALS3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094201
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer