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Fig. 10 | BMC Genomics

Fig. 10

From: Complexity of a small non-protein coding sequence in chromosomal region 22q11.2: presence of specialized DNA secondary structures and RNA exon/intron motifs

Fig. 10

Nucleotide sequence from Homo sapiens chromosome 22 (GRCh38 Primary Assembly, coordinates 18203085–18206244. Shown in red highlighted lettering are sequences that represent segments of the translocation breakpoint Type A sequence. The top 1–507 positions in the figure have an identity of 97 % with positions 310–814 on translocation breakpoint Type A but is present in the reverse complement. The bottom highlighted region, positions 2323–3100 in the figure have an identity of 96 % with position 310–1088 of translocation breakpoint Type A sequence, also in the reverse complement. The sequence highlighted in blue (positions 509–2200) represents the high A + T (93 %) region. The short unhighlighted sequence in black letters has not been characterized

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