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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.

View JSON schemaExpandCollapse
JSON · 12 lines · 252 chars

Examples (1)

Default NCBIVariation Spdi Canonical call

Public-safe example · rate-limited

JSON input · 3 lines · 42 chars
Expected response keys: success

Identifiers

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