A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267135



Internal ID20834175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109441919..109463204hg38UCSC Ensembl
chr5:108777620..108798905hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3821286
hg1921286
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267135
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