A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253575



Internal ID20820615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16108789..16132392hg38UCSC Ensembl
chr20:16089434..16113037hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3823604
hg1923604
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253575
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