Extended Data Fig. 3: Sequencing coverage in exome sequencing data.
From: De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
The number of sequencing reads covering the position of the n.64_65insT variant in 13,450 probands with exome sequencing in the DDD cohort. 3,408/13,450 probands (25.3%) have at least one read at the position.
