AnVIL
NHGRI Analysis Visualizationand Informatics Lab-space
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Study

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CCDG-Cardiovascular: University of Pennsylvania Cohort

CCDGphs001502.v1.p1dbGapdbGap FHIR

Description

The National Human Genome Research Institute (NHGRI) has funded the Centers for Common Disease Genomics (CCDG), a collaborative large-scale genome sequencing effort to comprehensively identify rare risk and protective variants contributing to multiple common disease phenotypes and to better understand the general principles of genomic architecture underlying common, complex inherited diseases.

This study of early onset cardiovascular disease and metabolic risk contains data derived from the whole genome sequence data of individuals participating in Penn Medicine's BioBank.

Stats

3Cohorts
2,256Samples
2,256Participants
44.93 TBSize

Summary

Consent CodesConsortia Access Only, TBD, HMB-IRB-PUB
Diseasesatrial fibrillation, coronary artery disease
AccessConsortium Access Only, Controlled Access
Study DesignCase Set, TBD, Case-Control
Data TypesWhole Genome, TBD

Terra Workspaces

This study has been divided into the following workspaces by consent codes and optionally the originating laboratory.

Terra Workspace NameConsent CodeDiseaseAccessStudy DesignData TypeSamplesParticipantsSize (TB)
AnVIL_CCDG_Broad_CVD_AFib_Penn_WGSConsortia Access Onlyatrial fibrillationCase SetWhole Genome4184188.56
AnVIL_CCDG_TOPMed_WashU_CVD_Afib_Penn_WGSTBDatrial fibrillationTBDTBD4824829.36
AnVIL_CCDG_WashU_CVD_EOCAD_Penn_WGSHMB-IRB-PUBcoronary artery diseaseCase-ControlWhole Genome1,3561,35627.01