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Cortexa research tool·genomics·ncbi_variation

NCBIVariation Spdi Canonical

Get the canonical (normalized) SPDI representation for a variant. Returns the single canonical form of a variant after normalization (right-shifting for indels, using the top-level chromosome sequence). Useful for variant deduplication and consistent storage.

AvailableCortexa

Schema

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

JSON · 12 lines · 252 chars

Examples (1)

Default NCBIVariation Spdi Canonical call

public-safeinput
JSON · 3 lines · 16 chars
Expected response keys: success

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

Identifiers

Catalog ID
tu_NCBIVariation_spdi_canonical
Tool name
NCBIVariation_spdi_canonical
Added
2026-05-01 00:58Z
Tags
tooluniverse
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