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Accession: PRJNA29893 ID: 29893

Homo sapiens (human)

Human Genome Structural Variation Project.

See Genome Information for Homo sapiens

The sequence-based survey of human genome structural variation aims to characterize common structural variants that are larger than SNPs, for example, multi-base insertions/deletions, inversions, translocations, and duplications. More...

AccessionPRJNA29893
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Publications
  • Kidd JM et al., "Mapping and sequencing of structural variation from eight human genomes.", Nature, 2008 May 1;453(7191):56-64
  • Tuzun E et al., "Fine-scale structural variation of the human genome.", Nat Genet, 2005 Jul;37(7):727-32
SubmissionRegistration date: 12-Nov-2003
Project Data:
Resource NameNumber
of Links
Sequence data
Nucleotide (Genomic DNA)6863
SRA Experiments679
Capillary Traces (Trace Archive)1
Publications
PubMed2
PMC1
Other datasets
BioSample8
Variation (dbVar)18751
SRA Data Details
ParameterValue
Data volume, Gbases86
Data volume, Tbytes0.97

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