A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237623



Internal ID20804663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89515139..89515748hg38UCSC Ensembl
chr14:89981483..89982092hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591031
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237623
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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