A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561890



Internal ID334857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107391212..107391290hg38UCSC Ensembl
chr3:107110059..107110137hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561890
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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