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Table 4 Autosomal common fragile sites, whose locations on the human genome sequence have been demarcated by flanking markers, and their overlap with evolutionary breakpoint intervals.

From: Gene synteny comparisons between different vertebrates provide new insights into breakage and fusion events during mammalian karyotype evolution

Fragile site [reference] Location in the human genome Overlap with evo breakpoint
  5' Boundary 3' Boundary  
  Marker designation Position (Mb) Marker designation Position (Mb)  
FRA2G [38] LASSG 169 PPJG 170.2 --
FRA3B [39] SHGC86352 59.7 RH41625 60.5 --
FRA4F [40] SNCA 90.8 MNC5C 96.7 95.62–95.73
FRA6E [41] D6S1581 160.2 D6S1719 165.9 --
FRA6F [42] SHGC144121 111.7 SHGC82095 112.7 --
FRA7E [43] D7S1934 80.3 SHGC104456 84.7 84.40–85.92
FRA7G [44] SHGC143971 115.6 RH44861 116.2 --
FRA7H [45] D7S614 130.2 STSG33535FS 130.4 --
FRA7I [46] SHGC153624 144.3 SWSS2627 145.7 --
FRA7K [47] IMMP22L 109.9 IMMP22L 110.7 --
FRA9E [48] D9S1866 106.9 D9S154 118.4 --
FRA16D [49] SHGC150973 76.7 WJ2755 77.8 --