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  2. Homologous chromosome - Wikipedia

    en.wikipedia.org/wiki/Homologous_chromosome

    Humans have a total of 46 chromosomes, but there are only 22 pairs of homologous autosomal chromosomes. The additional 23rd pair is the sex chromosomes, X and Y. Note that the pair of sex chromosomes may or may not be homologous, depending on the sex of the individual. For instance, females contain XX, thus have a homologous pair of sex ...

  3. Human genome - Wikipedia

    en.wikipedia.org/wiki/Human_genome

    The human genome is a complete set of nucleic acid sequences for humans, encoded as the DNA within each of the 24 distinct chromosomes in the cell nucleus. A small DNA molecule is found within individual mitochondria. These are usually treated separately as the nuclear genome and the mitochondrial genome. [ 1 ]

  4. Chromosomal translocation - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_translocation

    Chromosomal translocation. Chromosomal reciprocal translocation of the 4th and 20th chromosome. In genetics, chromosome translocation is a phenomenon that results in unusual rearrangement of chromosomes. This includes balanced and unbalanced translocation, with two main types: reciprocal, and Robertsonian translocation.

  5. Chromosome - Wikipedia

    en.wikipedia.org/wiki/Chromosome

    This is an accepted version of this page This is the latest accepted revision, reviewed on 15 October 2024. DNA molecule containing genetic material of a cell This article is about the DNA molecule. For the genetic algorithm, see Chromosome (genetic algorithm). Chromosome (10 7 - 10 10 bp) DNA Gene (10 3 - 10 6 bp) Function A chromosome and its packaged long strand of DNA unraveled. The DNA's ...

  6. Robertsonian translocation - Wikipedia

    en.wikipedia.org/wiki/Robertsonian_translocation

    The short arms of the chromosomes (shown on right) are often lost. Robertsonian translocation (ROB) is a chromosomal abnormality where the entire long arms of two different chromosomes become fused to each other. It is the most common form of chromosomal translocation in humans, affecting 1 out of every 1,000 babies born. [1]

  7. DNA - Wikipedia

    en.wikipedia.org/wiki/DNA

    The set of chromosomes in a cell makes up its genome; the human genome has approximately 3 billion base pairs of DNA arranged into 46 chromosomes. [96] The information carried by DNA is held in the sequence of pieces of DNA called genes .

  8. Gene - Wikipedia

    en.wikipedia.org/wiki/Gene

    A human DNA can have up to 500 million base pairs with thousands of genes. ... It shows 22 homologous chromosomes, both the male ... 6.2 Translation is carried out by ...

  9. Chromosomal crossover - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_crossover

    A double crossing over. Chromosomal crossover, or crossing over, is the exchange of genetic material during sexual reproduction between two homologous chromosomes ' non-sister chromatids that results in recombinant chromosomes. It is one of the final phases of genetic recombination, which occurs in the pachytene stage of prophase I of meiosis ...