A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697978



Internal ID121644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76768749..76772469hg38UCSC Ensembl
chr14:77235092..77238812hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg383721
hg193721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505173
Supporting Variants
Samples
Known GenesVASH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697978
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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