A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698334



Internal ID122000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102218644..102218723hg38UCSC Ensembl
chr14:102684981..102685060hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503471
Supporting Variants
Samples
Known GenesWDR20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698334
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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