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Chromosomes in a typical somatic human cell
46 chromosomes organized into 23 pairs.
Autosomes
Chromosomes other than sex chromosomes; humans have 44 autosomes.
Sex Chromosomes
Determine an individual's sex; humans have XX for females and XY for males.
Diploid cells
Cells that contain pairs of homologous chromosomes (2n); for humans, the diploid number is 46.
Haploid cells
Cells that contain a single set of chromosomes (n); for humans, the haploid number is 23.
Meiosis I
The first division in meiosis resulting in two haploid cells.
Meiosis II
The second division in meiosis, similar to mitosis, resulting in four haploid gametes.
Independent orientation of chromosomes
Chromosome pairs line up randomly in meiosis, contributing to genetic variation.
Crossing over
Exchange of segments between non-sister chromatids of homologous chromosomes during Prophase I.
Random fertilization
Any sperm can fertilize any egg, contributing to genetic variation among offspring.
Nondisjunction
Failure of chromosomes to separate properly during meiosis, leading to gametes with abnormal chromosome numbers.
Karyotyping
A process to visualize chromosomes for detecting abnormalities, such as genetic disorders.
Deletion
Removal of a segment of a chromosome.
Duplication
Copying a segment of a chromosome and inserting it into the homologous chromosome.
Inversion
A segment of a chromosome is removed and reinserted in the opposite orientation.
Reciprocal translocation
Segments of two nonhomologous chromosomes swap locations.