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Accession: PRJNA1103238 ID: 1103238

Homo sapiens (human)

Homo sapiens Variation

See Genome Information for Homo sapiens
Genomic copy number data and analysis from individuals with bicuspid aortic valves and unselected controls from the database of Genotypes and Phenotypes. Whole genome microarray genotyping and copy number variant calls on Illumina platforms.
AccessionPRJNA1103238
Data TypeVariation, Phenotype or Genotype
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsCarlisle SG et al., "Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve.", medRxiv, 2023 Oct 24;
Grants
  • "Genetic Basis of Early Onset Bicuspid Aortic Valve Disease" (Grant ID R01 HL137028, National Heart, Lung, and Blood Institute)
SubmissionRegistration date: 22-Apr-2024
University of Texas Health Science Center at Houston
RelevanceMedical
Project Data:
Resource NameNumber
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Publications
PubMed1
PMC1
No public data is linked to this project. Any recently released data that cites this project will be linked to it within a few days.

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