A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095754



Internal ID21275564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49790654..49791786hg38UCSC Ensembl
Innerchr13:50364790..50365922hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381133
hg191133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111327
Supporting Variants
Samplessample224
Known GenesKPNA3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095754
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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