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Accession: PRJNA503394 ID: 503394

Homo sapiens (human)

ACpop

See Genome Information for Homo sapiens
This dataset contains whole-genome variant frequencies for 300 individuals from Västerbotten County in Sweden, generated within the a project aimed to find variants giving a predisposition for cancer. More...
AccessionPRJNA503394
Data TypeGenome sequencing, Variation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 1-Nov-2018
Umea University
Project Data:
Resource NameNumber
of Links
BioSample1
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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