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Accession: PRJNA291948 ID: 291948

Homo sapiens (human)

Whole exome sequence of hearing loss family

See Genome Information for Homo sapiens
Our goal is to find genes responsible for non-syndromic sensorineural hearing loss. More...
AccessionPRJNA291948; dbGaP: phs000969
Data TypePhenotype or Genotype
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 5-Aug-2015
Albert Einstein College of Medicine
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments4
Other datasets
BioSample4
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases11
Data volume, Mbytes4572

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