A woman who sought genetic counseling is found to be heterozygous for a chromosomal rearrangement between the second and third chromosomes. Her chromosomes, compared to those in a normal karyotype, are diagrammed to the right. This woman is phenotypically normal. Does this surprise you? Why or why not? Under what circumstances might you expect a phenotypic effect of such a rearrangement?
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
6. Chromosomal Variation
Chromosomal Rearrangements: Translocations
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Join thousands of students who trust us to help them ace their exams!Watch the first videoMultiple Choice
Which type of chromosomal rearrangement occurs when part of a chromosome breaks off and attaches to a nonhomologous chromosome?
A
Deletion
B
Translocation
C
Inversion
D
Duplication

1
Understand the types of chromosomal rearrangements: Deletion involves loss of a chromosome segment; Inversion involves a segment breaking off and reattaching in reverse order on the same chromosome; Duplication involves a segment being copied and inserted into the chromosome.
Recognize that the problem describes a segment breaking off from one chromosome and attaching to a different, nonhomologous chromosome, which is a key feature of translocation.
Recall that translocation is the rearrangement where a chromosome segment moves to a nonhomologous chromosome, potentially altering gene location and function.
Differentiate translocation from other rearrangements by noting that it involves two different chromosomes exchanging or moving segments, unlike deletion, inversion, or duplication which occur within the same chromosome.
Conclude that the described event matches the definition of translocation, where a chromosome segment breaks off and attaches to a nonhomologous chromosome.
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