Natural genetic variation caused by small insertions and deletions in the human genome

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 1.
Figure 1.

Comparisons of our data with small INDELs identified from other projects. (A,B) Diagrams comparing the 1.96 million INDELs discovered in this study with the small INDELs that were identified in four personal genomes. (A) Comparison of our 1.96 million INDELs (light blue, top) with Venter (Levy et al. 2007) and Watson (Wheeler et al. 2008) INDELs. (B) Comparison of our 1.96 million INDELs (light blue, top) with Han Chinese (Wang et al. 2008) and Yoruban (Bentley et al. 2008) INDELs, (C) Comparison of our 1.96 million INDELs (light blue, top) with the 1.48 million INDELs identified by the 1000 Genomes Project (1000GP) (The 1000 Genomes Project Consortium 2010).

This Article

  1. Published in Advance April 1, 2011, doi: 10.1101/gr.115907.110 Genome Res. 21: 830-839

Preprint Server



Current Issue

  1. March 2026, 36 (3)
  1. Current Issue
  1. Alert me to new issues of Genome Research