A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696421



Internal ID120087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57025592..57039855hg38UCSC Ensembl
chr14:57492310..57506573hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3814264
hg1914264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497379
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696421
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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