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    • SPDI Variation Service

    Metadata Updated: October 1, 2022

    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 October 1, 2022

    Metadata Source

    Harvested from Healthdata.gov

    Other Data Resources

    Additional Metadata

    Resource Type Dataset
    Metadata Created Date July 3, 2021
    Metadata Updated Date October 1, 2022
    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 2022-09-30
    Category Molecular biology/Genetics
    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 747f1dde-7407-4f91-a68c-dd7a0bf5dc57
    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 5f811ba47f59ea4365e5979b2efa86812f11c474
    Source Schema Version 1.1

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