A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233299



Internal ID20800339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20216092..22917423hg38UCSC Ensembl
chr13:20790231..23491562hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382701332
hg192701332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587146
Supporting Variants
Samples
Known GenesBASP1P1, CRYL1, FGF9, GJB6, IFT88, IL17D, LATS2, LINC00367, LINC00424, LINC00539, LINC00540, MICU2, MIPEPP3, MIR4499, MRP63, N6AMT2, SAP18, SKA3, XPO4, ZDHHC20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233299
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