This page is part of the Genetic Reporting Implementation Guide (v3.0.0: STU3) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
Generated Narrative: Observation ExampleSomaticDEL
status: Final
category: Laboratory, Genetics
code: Genetic variant assessment
subject: Adam B. Everyman Male, DoB: 1951-01-20 ( Medical Record Number: m123 (use: usual, ))
effective: 2019-04-01
performer: Organization some lab
value: Present
method: Sequencing
component
code: DNA change type
value: deletion
component
code: Genomic ref allele [ID]
value: C
component
code: Genomic source class [Type]
value: Somatic
component
code: Genomic reference sequence [ID]
value: NC_000001.10
component
code: Genomic structural variant copy number
value: 1 1 (Details: UCUM code1 = '1')
component
code: Genomic coordinate system [Type]
value: 1-based character counting
component
code: Structural variant inner start and end
value: 16360078-16383337