the male chromosome is XY
the female chromosome is XX
The paired chromosomes that determine an individual's gender are called sex chromosomes.
Body cells typically have a diploid number of chromosomes, meaning they have two sets of chromosomes. Sex cells, or gametes, have a haploid number of chromosomes, meaning they have one set of chromosomes. This allows for the correct number of chromosomes to be restored upon fertilization.
An organism with 24 chromosomes in each body cell will produce sex cells with 12 chromosomes each. This is because during meiosis, the chromosome number is halved to ensure the correct number of chromosomes in the offspring.
Humans have one pair of sex chromosomes. They are called X and Y. The two determine what sex a person will be. Males have X + Y and females have X + X. There are some genes that are called sex linked genes found on these. The Y chromosome is very small and contains mainly the genes that make a person a male. There are few other genes on the Y.
It depends on the species of hamster! Syrian hamsters (Mesocrictus auratus) have 21 pairs and two sex chromosomes (44 in total). Chinese hamsters (Cricetus griseus) have 10 pairs of chromosomes and two sex chromosomes (22 in total).
Except for the sex chromosomes paired chromosomes are homologs.
The paired chromosomes that determine an individual's gender are called sex chromosomes.
They are paired. Males have XY as a pair and females have XX as pairs.
yes,in the somatic cells.But not in the reproductive cells
looks like a complex network of chromatin
Autosomes are the non-sex chromosomes. The 23rd pair is the sex chromosomes. Autosomal homologous pairs are all shaped like Xs. The sex chromosomes, as we know, can either be XX or XYType your answer here...
All the autosomes are paired but the sex chromosome of a number of animals are not paired and they reproduce successfully.
Body cells typically have a diploid number of chromosomes, meaning they have two sets of chromosomes. Sex cells, or gametes, have a haploid number of chromosomes, meaning they have one set of chromosomes. This allows for the correct number of chromosomes to be restored upon fertilization.
autosomal chromosomes carry diverse info sex chromosomes determine an individual's sex ---- ok, that is some other dude's answer, now here is mine: the autosomal is all the chromosomes, except for the sex chromosomes. so, in a sense, the autosomal has nothing to do with the sex chromosomes. sex chromosomes determine the offspring's sex, as the guy above said it. autosomal is simply all of the other chromosomes ----- For A+ the answer is "Autosomal chromosomes carry diverse information; sex chromosomes determine an individual's sex."
Human cells have 23 distinct types of chromosomes, including the 22 autosomes and the X or Y sex chromosome. (The autosomes are usually paired and are the same in both sexes.) You inherit one of each type from each of your parents so that the typical human somatic cell has 46 chromosomes. (Sperm and egg cells, of course, have 23 each.) While there is no difference in the 44 autosomnal chromosomes by sex, the sex chromosomes are paired XX in a woman and XY in a man.
An autosome is a non-sex chromosome. It is an ordinarily paired type of chromosome that is the same in both sexes of a species. For example, in humans, there are 22 pairs of autosomes. The X and Y chromosomes are not autosomal. Non-autosomal chromosomes are usually referred to as sex chromosomes, allosomes or heterosomes.
A display of homologous pairs and sex chromosomes is typically represented in a karyotype, which is a systematic arrangement of an organism's chromosomes. In a karyotype, chromosomes are paired based on their size, shape, and banding patterns, with homologous pairs showing similar characteristics. The sex chromosomes, which determine the biological sex of an organism, are usually represented as X and Y chromosomes in humans, with females having two X chromosomes (XX) and males having one X and one Y chromosome (XY). This visual representation aids in identifying chromosomal abnormalities and understanding genetic traits.