A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697137



Internal ID120803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89461291..89472663hg38UCSC Ensembl
chr14:89927635..89939007hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3811373
hg1911373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501998
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697137
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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