R4 Ballot #1 #2 (Mixed Normative/Trial use)

This page is part of the FHIR Specification (v3.3.0: (v3.5.0: R4 Ballot 2). #2). The current version which supercedes this version is 5.0.0 . For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B R4 R3

Sequence-complex-variant

Clinical Genomics Work Group Maturity Level : N/A Ballot Status : Informative Compartments : Not linked to any defined compartments

This is the narrative for the resource. See also the XML or , JSON or Turtle format. This example conforms to the profile Sequence .

Generated Narrative with Details

id : sequence-complex-variant

identifier : ?? (OFFICIAL)

type : dna

coordinateSystem : 1

specimen : Molecular Specimen ID: MLD45-Z4-1234

device : 12 lead EKG Device Metric

performer : HL7

quantity : 25

ReferenceSeqs

- ReferenceSeqId Strand WindowStart WindowEnd
* NC_000002.12 (Details : {http://www.ncbi.nlm.nih.gov/nuccore code 'NC_000002.12' = 'NC_000002.12) watson 128273724 128273754

Variants

- Start End ObservedAllele ReferenceAllele Cigar
* 128273724 128273736 CTCATTGT CTCCATTGCATGCGTT 3M1D4M6N2M

readCoverage : 1

Repositories

- Type DatasetId ReadsetId
* other Ensembl v1beta2

 

 

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.