A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225798



Internal ID20792838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102806495..102806922hg38UCSC Ensembl
chr13:103458845..103459272hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582238
Supporting Variants
Samples
Known GenesBIVM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225798
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