SPDI Variation Service

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

Data e Risorse

Campo Valore
accessLevel public
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identifier https://datadiscovery.nlm.nih.gov/api/views/jy6x-w83b
issued 2021-06-30
landingPage https://api.ncbi.nlm.nih.gov/variation/v0/
license http://opendefinition.org/licenses/odc-odbl/
modified 2022-05-25
programCode {009:041}
publisher National Library of Medicine
resource-type Dataset
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Gruppi
  • AmeriGEOSS
  • National Provider
  • North America
Tag
  • amerigeo
  • amerigeoss
  • api
  • ckan
  • data-specifications
  • genetics
  • genomics
  • geo
  • geoss
  • molecular-biology
  • national
  • north-america
  • tools-utilities
  • united-states
isopen False
license_id other-license-specified
license_title other-license-specified
maintainer National Library of Medicine
maintainer_email custserv@nlm.nih.gov
metadata_created 2025-11-22T17:20:03.628423
metadata_modified 2025-11-22T17:20:03.628426
notes 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
num_resources 1
num_tags 14
title SPDI Variation Service