A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233392



Internal ID20800432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98805765..98806923hg38UCSC Ensembl
chr13:99458019..99459177hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381159
hg191159
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591431
Supporting Variants
Samples
Known GenesDOCK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233392
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