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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...

Project Type:Clone ends, Genome sequencing, Variation
Attributes:Scope: Multiisolate; Material: Genome; Capture: Clone Ends; Method type: Sequencing
Project Data:
Resource NameNumber
of Links
Sequence data
Nucleotide (Genomic DNA)6865
SRA Experiments6
Capillary Traces (Trace Archive)1
Publications
PubMed1
PMC1
Other datasets
BioSample3
Variation (dbVar)18751
SRA Data Details
ParameterValue
Data volume, Gbases63
Data volume, Mbytes55514
Publications:
  • Kidd JM et al., "Mapping and sequencing of structural variation from eight human genomes.", Nature, 2008 May 1;453(7191):56-64
Submission:

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