Study Description

Copy number variation (CNV) has been recognized as a major contributor to human genome diversity. It plays an important role in... Show More

Study Accession Alternative Stable ID type
phs000664.v1.p1 dbGaP Population

Who controls access to this study

National Human Genome Research Institute
Access information:


Data provider(s)

  • Title Name Institute
    Principal Investigator Boon Peng Hoh Institute of Medical Molecular Biology, (IMMB), Faculty of Medicine, Universiti Teknologi MARA, Sg Buloh Campus, Malaysia

Who archives the data?

The database of Genotypes and Phenotypes (dbGaP)