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Research tool·genomics·ensembl
Ensembl Get Structural Variants
Get structural variants overlapping a genomic region from Ensembl. Returns known SVs from DGVa (Database of Genomic Variants archive), ClinGen, and other sources. Each SV includes its ID (nsv/esv accession), coordinates, and feature type. Use ensembl_get_sv_detail to get clinical significance, variant class (CNV, deletion, duplication, inversion), and supporting evidence for specific variants. Region must be < 5Mb.
AvailableCortexa
Schema
JSON Schema the agent (or your API call) must match.
View JSON schemaExpandCollapse
JSON · 22 lines · 551 chars
Examples (1)
Default Ensembl Get Structural Variants call
Public-safe example · rate-limited
JSON input · 5 lines · 97 chars
Expected response keys: success
Identifiers
- Catalog ID
- tu_ensembl_get_structural_variants
- Tool name
- ensembl_get_structural_variants
- Added
- 2026-05-01 00:58Z
- Tags
- tooluniverse