A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237388



Internal ID20804428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64470334..64471302hg38UCSC Ensembl
chr14:64937052..64938020hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595170
Supporting Variants
Samples
Known GenesAKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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