Known IssuesΒΆ
| Issue | Fix Version |
|---|---|
| SV plot arcs are not readjusting on the y-axis when zooming into the breakpoints | 5.0.0 |
| Structural variants in the variant list are absent from the structural variant plot | 5.0.0 |
| Gene names are being hidden when resizing the domain column in the variant list | 5.0.0 |
| Both IGV links for SVs on the variant list point to the first breakpoint | 5.0.0 |
| History of the validation and artefact assessment is not displaying correctly in the Variant List | TBC |
| Tooltip is not getting displayed for Origin in variant Details (Structural Variants) | TBC |
| The line representing the median is being obscured by the reference line in the SV and CNV plots | TBC |
| Cancer Hotspots are not yet available for splice variants or Indels | TBC |
| Tumour morphology and topography is not displayed correctly in the case summary | TBC |
| Option to sort somatic small variants by VAF is missing in the variant list | TBC |
| Tooltip for QC flag column name and values in the germline small variant list is not visible | TBC |
| Split read value is empty if no data we should not display the field in structural variant | TBC |
| Paired reads are not getting displayed if Split read is not available in the data | TBC |
| The gene track doesn't display properly when the are no genes matching the patient clinical indication | TBC |
| Clicking on an empty region of the SV chart removes all results from the corresponding variant list | TBC |
| The value for paired or split reads shows as 'Not applicable' for SVs with no SR/PR support | TBC |
Please report any bugs or issues with the DSS via the Genomics England Service Desk. We will log these bugs
Last update:
2023-10-03