A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022672



Internal ID20589712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89546892..89591866hg38UCSC Ensembl
chr14:90013236..90058210hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3844975
hg1944975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511639
Supporting Variants
Samples
Known GenesFOXN3, FOXN3-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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