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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

2Cohorts
1,774Samples
1,774Participants
35.56 TBSize

Summary

Consent CodesHMB-IRB-PUB
Diseasesatrial fibrillation, coronary artery disease
AccessControlled Access
Study DesignCase-Control
Data TypesWhole Genome

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_WGSHMB-IRB-PUBatrial fibrillationCase-ControlWhole Genome4184188.56
AnVIL_CCDG_WashU_CVD_EOCAD_Penn_WGSHMB-IRB-PUBcoronary artery diseaseCase-ControlWhole Genome1,3561,35627.00