It'd be good to pull out these panels, parse ISCA IDs/SV type, and go looking for matching variants in our SV data. This could be treated as a variant whitelist category.
Side note.... does Clinvar have SVs in a format that's easy to pull down and annotate against our variant data
e.g. https://panelapp.agha.umccr.org/panels/3443/
It'd be good to pull out these panels, parse ISCA IDs/SV type, and go looking for matching variants in our SV data. This could be treated as a variant whitelist category.
Side note.... does Clinvar have SVs in a format that's easy to pull down and annotate against our variant data