Cortexa research tool·genomics·ensembl

Ensembl Get Sv Detail

Get detailed information for a specific structural variant from Ensembl by its accession (nsv/esv ID). Returns variant class (CNV, deletion, duplication, inversion, gain, loss), clinical significance (pathogenic, benign, etc.), source database, supporting evidence with individual sample observations, study information, and genomic mappings. Essential for CNV clinical interpretation.

Livelast probed 2026-04-30 23:07Z· 108msCortexa

Status

The most recent probe succeeded. Safe to call from the agent today.

Last probed: 1d ago
Last success: 1d ago
Last latency: 108ms

Schema

JSON Schema the agent (or your API call) must match.

{
  "properties": {
    "id": {
      "description": "Structural variant accession from Ensembl/DGVa (e.g., 'nsv2769779', 'esv3647486'). Use ensembl_get_structural_variants to find IDs.",
      "type": "string"
    },
    "species": {
      "default": "human",
      "description": "Species name (e.g., 'human', 'homo_sapiens').",
      "type": "string"
    }
  },
  "required": [
    "species",
    "id"
  ],
  "type": "object"
}

Examples (1)

Default Ensembl Get Sv Detail call

public-safeinput

{
  "id": "",
  "species": ""
}

Expected response keys: success

Anonymous-safe example. Rate-limited; no sign-in required.

Identifiers

Catalog ID: tu_ensembl_get_sv_detail
Tool name: ensembl_get_sv_detail
Added: 2026-04-30 22:47Z
Tags: tooluniverse

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