A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218399



Internal ID20785439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109173652..109174707hg38UCSC Ensembl
chr13:109826000..109827055hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576765
Supporting Variants
Samples
Known GenesMYO16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218399
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