A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252792



Internal ID20819832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97799603..97805152hg38UCSC Ensembl
chr1:98265159..98270708hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg385550
hg195550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554534
Supporting Variants
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252792
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00036


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