Table 2 Number of identified SNVs and indels

From: A practical method to detect SNVs and indels from whole genome and exome sequencing data

Number

WGS

WES

Total SNVs

3,406,875

79,060

Total indels *

763,944 (106,732)

10,999

Total SNVs in splice sites

105

56

Total SNVs in coding region

20,314

19,861

Missense

9,502

9,360

Nonsense

109

83

Synonymous

10,703

10,418

Total indels in coding region

461

509

  1. *: In the WGS, the numbers of indels in all region and non-repeat regions are shown.