JBrowse 2 has a special "view type" called the "breakpoint split view" that allows you to see the connection between split long reads (e.g. SA tag) and paired-end reads
The SV inspector lets you load a VCF containing SV calls and then will launch a "breakpoint split view". Note that the breakpoint split view that it launches will be empty but you can then add your BAM or CRAM reads to it (on both top and bottom levels sometimes is needed)
Fig1. Clicking on a "chord" of the SV inspector
Fig2. Clicking on the dropdown menu of the SV inspector. Note that it gives the option for "top/bottom" and "single row"
Recent versions added the ability to launch th breakpoint split view directly from the "feature details" of an alignments feature or variant feature
Fig3. The feature details from clicking on a long read in a plain old linear genome view with links to "Launch split view". Note that it gives the option for "top/bottom" and "single row"
Fig4. The feature details from clicking on a variant call in a plain old linear genome view with links to "Launch split view". Note that it gives the option for "top/bottom" and "single row"
- The top/bottom "mode" of the breakpoint split view stracks two independent linear genome view vertically.
- The single row "mode" is split "left/right" in a single linear genome view