A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697325



Internal ID120991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99017512..99025821hg38UCSC Ensembl
chr14:99483849..99492158hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388310
hg198310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503928
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697325
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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