A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602597



Internal ID21794644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35233087..35233672hg38UCSC Ensembl
chr14:35702293..35702878hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038147
Supporting Variants
Samples
Known GenesKIAA0391
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602597
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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