A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226822



Internal ID20793862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49059515..49060564hg38UCSC Ensembl
chr13:49633651..49634700hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588314
Supporting Variants
Samples
Known GenesFNDC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226822
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