A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697993



Internal ID121659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76977048..76979392hg38UCSC Ensembl
chr14:77443391..77445735hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382345
hg192345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697993
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.014674


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