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A human cell typically contains 46 chromosomes.
Chromosomes are thread-like structures located inside the nucleus of animal and plant cells. Each chromosome is made of protein and a single molecule of deoxyribonucleic acid (DNA), which carries the cell's genetic instructions. In humans, cells normally contain 46 chromosomes, which come in 23 pairs. One pair, the sex chromosomes, determines a person's sex: females have two X chromosomes (XX), while males have one X and one Y chromosome (XY).
The other 22 pairs of chromosomes are known as autosomes, and they carry the bulk of the genetic material. These chromosomes are numbered from 1 to 22, with chromosome 1 being the largest and chromosome 22 the smallest. Each chromosome carries hundreds to thousands of genes; these genes contain the instructions for building proteins, which perform a vast array of functions in the body.
When a cell divides, it must replicate its DNA so that each new cell gets a complete set of chromosomes. This process is called DNA replication. Errors in this process can lead to mutations, which can cause genetic disorders or contribute to the development of diseases like cancer.
It's also worth noting that there are exceptions to the typical number of 46 chromosomes. Some people have different numbers of chromosomes due to conditions like Down syndrome, which is caused by an extra copy of chromosome 21, or Turner syndrome, which occurs when a female has only one X chromosome. Despite these variations, the vast majority of human cells contain 46 chromosomes.
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