A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697121



Internal ID120787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89174007..89176056hg38UCSC Ensembl
chr14:89640351..89642400hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg382050
hg192050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497824
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697121
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001873


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