Figure 2
From: Whole genome and exome sequencing of monozygotic twins discordant for Crohn’s disease
Screenshot from IGV at a position called as a significant difference between the blood sample and biopsy exomes of the affected twin from TP1 (SNV2). The alignment shows another SNV (SNV1) and an insertion nearby. Realignment of one read each shows identical alignability to the reference by introduction of a 19 bp insertion.