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Accession: PRJNA481779 ID: 481779

Homo sapiens (human)

Characterizing the major structural variant alleles of the human genome

See Genome Information for Homo sapiens
The reference genome plays a critical role in science and medicine, and despite decades of development, it still contains errors, rare alleles, and missing sequence. More...
AccessionPRJNA481779
Data TypeGenome sequencing and assembly
ScopeMultispecies
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Grants
  • "Sequence and Assembly of Segmental Duplications" (Grant ID R01 HG002385, National Human Genome Research Institute)
  • "HIGH QUALITY HUMAN AND NON-HUMAN PRIMATE GENOME ASSEMBLIES" (Grant ID U24 HG009081, National Human Genome Research Institute)
  • "HIGH QUALITY HUMAN AND NON-HUMAN PRIMATE GENOME ASSEMBLIES" (Grant ID U24 HG009081, National Human Genome Research Institute)
  • "Improving the Human Reference Genome Resource" (Grant ID U41 HG007635, National Human Genome Research Institute)
  • "A Platform for Large-Scale Genomic Discovery" (Grant ID U54 HG003079, National Human Genome Research Institute)
  • "A Platform for Large-Scale Genomic Discovery" (Grant ID U54 HG003079, National Human Genome Research Institute)
SubmissionRegistration date: 2-Nov-2018
University of Washington
RelevanceEvolution
Project Data:
Resource NameNumber
of Links
Sequence data
Nucleotide (WGS master)14
Other datasets
BioSample14
Variation (dbVar)99811
Assembly14

Supplemental Content

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  • Homo sapiens
    Homo sapiens
    Characterizing the major structural variant alleles of the human genome
    BioProject
  • PRJNA481779 (1)
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