About This Tool
This is a custom-built genome visualization tool for viewing structural variants and complex alignments. Upload your genomic data files to visualize:
- Structural variants (deletions, insertions, duplications, inversions)
- Long-read alignments
- Gene fusions and translocations
- Assembly-to-assembly comparisons
Controls
Supported: SAM, BAM, BED, VCF, or tab-delimited text
File Information
Genome Ribbon View
Click and drag to pan • Scroll to zoom • Click on features for details
Legend
Normal Alignment
Deletion
Insertion
Inversion
Duplication
Translocation
Gene Fusion
Unknown