U.S. flag

An official website of the United States government

Display Settings:

Format

Send to:

Choose Destination
Accession: PRJEB35772 ID: 605388

Homo sapiens (human)

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank

See Genome Information for Homo sapiens
Calling deletions covering the full region of 15q11.2 in the UK Biobank cohort of ~500,000 individuals and determining the region's association with cardiovascular and neurodevelopmental phenotypes
AccessionPRJEB35772
Data TypeVariation
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 7-Feb-2020
- European Bioinformatics Institute
- Bernard Keavney
Project Data:
Resource NameNumber
of Links
Variation (dbVar)242

Supplemental Content

Recent activity

  • Homo sapiens
    Homo sapiens
    Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank
    BioProject

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center