A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260743



Internal ID20827783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45203564..45204607hg38UCSC Ensembl
chr3:45245056..45246099hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381044
hg191044
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553325
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260743
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