A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239287



Internal ID20806328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55760563..55833133hg38UCSC Ensembl
chr16:55794475..55867045hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3872571
hg1972571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589659
Supporting Variants
Samples
Known GenesCES1, CES1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239287
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0165


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer