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Specification:

FHIR Core (FHIR)
Raised in Version:

STU3
Work Group:

Clinical Genomics
Related URL:
http://hl7.org/fhir/sequence-definitions.html#Sequence.readDepth
Related Artifact(s):

MolecularSequence (was Sequence)
Resolution Description:

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We are limiting attributes like this on the resource. This can be found on the Variant profile in the Genomics Reporting IG:
http://build.fhir.org/ig/HL7/genomics-reporting/StructureDefinition-variant-definitions.html#Observation.component:allelic-read-depth

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We are limiting attributes like this on the resource. This can be found on the Variant profile in the Genomics Reporting IG: http://build.fhir.org/ig/HL7/genomics-reporting/StructureDefinition-variant-definitions.html#Observation.component:allelic-read-depth
Resolution Vote:
Kevin Power / Patrick Werner : 13 - 0 - 0

Read depth information. 0..1, integer.

Mapping from V2 field "Allelic read depth"