How to identify structural variants (SV) breakpoints using alignment PAF file?

Question

[BioinfoBee]

Hello All, I have a minimap2 aligned .paf file of two genomes. This paf file was used to identify structural variant (SVs) shared between these genomes. How do I use this paf file alone for a precise detection of SV breakpoints?

Thank you for your time and feedback in advance.

Regards, B