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SPDI Variation Service

Metadata Updated: June 19, 2025

This genetic variation services interconvert and transform short genetic variants between HGVS expressions, VCF format, and the new SPDI (Sequence Position Deletion Insertion) format, based on alignment datasets used by ClinVar and dbSNP. NOTE: This service is still in beta testing mode

Access & Use Information

Public: This dataset is intended for public access and use. License: See this page for license information.

Downloads & Resources

Dates

Metadata Created Date July 3, 2021
Metadata Updated Date June 19, 2025

Metadata Source

Harvested from Healthdata.gov

Additional Metadata

Resource Type Dataset
Metadata Created Date July 3, 2021
Metadata Updated Date June 19, 2025
Publisher National Library of Medicine
Maintainer
Identifier https://datadiscovery.nlm.nih.gov/api/views/jy6x-w83b
Data First Published 2021-06-30
Data Last Modified 2025-06-18
Category Biology
Public Access Level public
Bureau Code 009:25
Metadata Context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
Metadata Catalog ID https://healthdata.gov/data.json
Schema Version https://project-open-data.cio.gov/v1.1/schema
Catalog Describedby https://project-open-data.cio.gov/v1.1/schema/catalog.json
Harvest Object Id 9d148a38-11d7-423b-ac08-0ee71c15fd75
Harvest Source Id 651e43b2-321c-4e4c-b86a-835cfc342cb0
Harvest Source Title Healthdata.gov
Homepage URL https://api.ncbi.nlm.nih.gov/variation/v0/
License http://opendefinition.org/licenses/odc-odbl/
Program Code 009:041
Source Datajson Identifier True
Source Hash 0973280e59c5e2c08a77e985c5a75a90e52e84bd700198a9a15b1a6e4b575966
Source Schema Version 1.1

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