A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602149



Internal ID21794196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89267464..89273922hg38UCSC Ensembl
chr14:89733808..89740266hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg386459
hg196459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023970
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602149
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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