A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253460



Internal ID20820500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60754714..60755760hg38UCSC Ensembl
chr20:59329771..59330817hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253460
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