Combined visualization of both SNV and SV/CNV for specific genes.

[xiamaz]

A common usage scenario is to quickly check whether for a certain gene where a variant of interest has been detected, additional variants might exist. While a comp het filter exists for SNV, such a feature is still missing for showing SV and CNV.

@holtgrewe Is this already something that is planned? Otherwise, I can further detail what we might want for that feature.

[holtgrewe]

Do #573 or #574 help?

[xiamaz]

Thanks! This should sufficiently cover this requirement for now.