Connectathon 11 Snapshot

This page is part of the FHIR Specification (v1.2.0: STU 3 Draft). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions

Sequence-genetics-example4

This is the narrative for the resource. See also the XML or JSON format.

Generated Narrative with Details

id: seq4

type: DNA

variationID: essv25820997 (Details : {http://www.ncbi.nlm.nih.gov/dbvar/ code 'essv25820997' = '??)

referenceSeq: NC_000007.14 (Details : {http://www.ncbi.nlm.nih.gov/nuccore/ code 'NC_000007.14' = '??)

Coordinates

-

Chromosome

Start

End

GenomeBuild

*

7 (Details : {[not stated] code '7' = '??)

87627621

87642522

GRCh38 (Details )

species: Homo sapiens (Details : {SNOMED CT code '337915000' = '??)

copyNumberEvent: deletion (Details )

Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.