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Cortexa 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.
Livelast probed 2026-05-01 01:00Z· 629msCortexa
Status
The most recent probe succeeded. Safe to call from the agent today.
- Last probed
- 1d ago
- Last success
- 1d ago
- Last latency
- 629ms
Schema
JSON Schema the agent (or your API call) must match.
{
"properties": {
"feature": {
"default": "structural_variation",
"description": "Feature type to retrieve. Fixed to 'structural_variation' for this tool.",
"type": "string"
},
"region": {
"description": "Genomic region in format 'chr:start-end' (e.g., '17:43044295-43125370'). Maximum 5Mb.",
"type": "string"
},
"species": {
"default": "human",
"description": "Species name (e.g., 'human', 'homo_sapiens').",
"type": "string"
}
},
"required": [
"species",
"region"
],
"type": "object"
}Examples (1)
Default Ensembl Get Structural Variants call
public-safeinput
{
"region": "",
"species": ""
}Expected response keys: success
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- tu_ensembl_get_structural_variants
- Tool name
- ensembl_get_structural_variants
- Added
- 2026-05-01 00:58Z
- Tags
- tooluniverse