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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
Complete Metadata
| bureauCode |
[ "009:25" ] |
|---|---|
| identifier | https://datadiscovery.nlm.nih.gov/api/views/jy6x-w83b |
| issued | 2021-06-30 |
| landingPage | https://api.ncbi.nlm.nih.gov/variation/v0/ |
| programCode |
[ "009:041" ] |
| theme |
[ "Biology" ] |
