A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226435



Internal ID20793475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23317915..23318221hg38UCSC Ensembl
chr14:23787124..23787430hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589154
Supporting Variants
Samples
Known GenesBCL2L2-PABPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226435
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