Fig. 2From: Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatiguePart of the 60 × coverage Oxford Nanopore sequence viewed in IGV. Multiple reads at each end of the region show a pattern of insertions, deletions and mismatched bases suggestive of a heterozygous structural variant but there are no split readsBack to article page