A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236267



Internal ID20803307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45496773..45497506hg38UCSC Ensembl
chr13:46070908..46071641hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583241
Supporting Variants
Samples
Known GenesCOG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236267
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