A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697122



Internal ID120788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89204983..89204983hg38UCSC Ensembl
chr14:89671327..89671327hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541384
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697122
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.036776


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