A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593943



Internal ID20967014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55289651..55290371hg38UCSC Ensembl
chr14:55756369..55757089hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237814
Samples
Known GenesFBXO34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593943
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer