A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698796



Internal ID122462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100357562..100357615hg38UCSC Ensembl
chr14:100823899..100823952hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510164
Supporting Variants
Samples
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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