I need some clarification on centromeres. I've tried Googling, but the level of technical jargon is beyond me. Do centromeres appear at various places on the chromosome, or just where the two sides cross over/meet? In terms of the Chromosome Browser, are the centromeres represented by the gray areas as well as the narrowing areas where the two "sides" meet?
The second half of my wondering is in regard to this comment found on another message board: Speaking about Chromosome 9, "Some people have an inversion there, which can prevent recombination and cause the segment to persist longer than usual. If you have an unusual number of matches in that vicinity, that might be an explanation." I do have a large number of FF matches on Chromosome 9--all overlapping. The matches are NOT on/overlapping the centromere/center areas, however. Does anyone know anything about this Chromosome 9 inversion, or can you point me to a layman's explanation?
The second half of my wondering is in regard to this comment found on another message board: Speaking about Chromosome 9, "Some people have an inversion there, which can prevent recombination and cause the segment to persist longer than usual. If you have an unusual number of matches in that vicinity, that might be an explanation." I do have a large number of FF matches on Chromosome 9--all overlapping. The matches are NOT on/overlapping the centromere/center areas, however. Does anyone know anything about this Chromosome 9 inversion, or can you point me to a layman's explanation?
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