A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107923



Internal ID21280902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190118019..190121259hg38UCSC Ensembl
Innerchr3:189835808..189839048hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg383241
hg193241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111093
Supporting Variants
Samplessample303
Known GenesLEPREL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107923
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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