sex chromosomes
Sex chromosomes X and Y are not homologous in a normal karyotype. This pair of chromosomes determines an individual's biological sex, with females having two X chromosomes and males having one X and one Y chromosome.
The question is not really clear. A karyotype is the overall complement of chromosomes isolated from a cell or organism (eukaryotic). When the karyotype of a normal healthy female is prepared for viewing by a cytogeneticist, there are 22 pairs of autosomal chromosomes present (ie two of chromosome 1, two of chromosome 2 etc...). There is one additional pair of sex chromosomes (two copies of X). A normal healthy human male also has 22 pairs of autosomes but the pair of sex chromosomes is not matched but instead there is one X chromosome and one Y chromosome (which is smaller than the X). So, if you look at a karyotype that has been laid out - if the two sex chromosomes are different sizes (X and Y) then the karyotype is from a male, if however they are the same size (X and X) then the karyotype is from a female.
A human gamete does not have any pairs of homologous chromosomes. A single human gamete contains 23 chromosomes, or a half set. None of these chromosomes are homologous with each other.
The chart used to determine a person's sex is called a karyotype chart. This chart displays the chromosomes found in an individual's cells, which can help determine their biological sex based on the presence of XX (female) or XY (male) chromosomes.
The word that describes similar chromosomes, one from each parent is homologous. Each human for example has, with certain exceptions 23 chromosome pairs. Twenty two are called autosomal meaning having basically to do with the body. These pairs are homologous. The remaining are the sex chromosomes, X and Y. Homologous chromosomes have the potential to contain exactly the same genes, but nature has made sure that they don't.
Sex chromosomes X and Y are not homologous in a normal karyotype. This pair of chromosomes determines an individual's biological sex, with females having two X chromosomes and males having one X and one Y chromosome.
The male karyotype has 46 chromosomes the same as the female karyotype:23 chromosomes are inherited from your father.
A karyotype will consist of all the homologous pairs of chromosomes and also one pair of chromosomes representing the sex of the organism (male/female). In Humans, a karyotype will consist of 22 homologous pairs of chromosomes and 1 pair of either XX or XY chromosomes. The total number of homologous pairs of chromosomes depends largely upon which organism is being taken into account, since each organism has its characteristic number of chromosomes in a diploid cell - in humans this is 46.
Yes. A karyotype will show the chromosomes and an affected person will have XXY instead of XY for a normal male.
No. A karyotype is an arrangement of the 22 pairs of homologous chromosomes and the 2 sex chromosomes according to their size and shape. The chromosomes are photographed during metaphase of mitosis and then arranged by a trained technologist. Karyotypes are determined in order to check for chromosomal abnormalities. Refer to the related links to see examples of a karyotype for a female and one for a male.
The question is not really clear. A karyotype is the overall complement of chromosomes isolated from a cell or organism (eukaryotic). When the karyotype of a normal healthy female is prepared for viewing by a cytogeneticist, there are 22 pairs of autosomal chromosomes present (ie two of chromosome 1, two of chromosome 2 etc...). There is one additional pair of sex chromosomes (two copies of X). A normal healthy human male also has 22 pairs of autosomes but the pair of sex chromosomes is not matched but instead there is one X chromosome and one Y chromosome (which is smaller than the X). So, if you look at a karyotype that has been laid out - if the two sex chromosomes are different sizes (X and Y) then the karyotype is from a male, if however they are the same size (X and X) then the karyotype is from a female.
The first 22 pairs of chromosomes in a karyotype are called autosomes. These chromosomes are numbered from 1 to 22, with each pair containing one chromosome inherited from each parent. They determine an individual's genetic characteristics and traits, excluding sex-linked traits.
A male's karyotype typically consists of 22 pairs of autosomal chromosomes and one pair of sex chromosomes, XY. The chromosomes would be arranged from largest to smallest, with the sex chromosomes at the end. So, the karyotype for a male would show 46 chromosomes, arranged with the XY sex chromosomes in the 23rd pair.
chromosomes having centromere of same size and position
The sex of an individual can be determined by analyzing the karyotype for the presence of sex chromosomes. A karyotype with two X chromosomes is typically female (XX), while a karyotype with one X and one Y chromosome is typically male (XY). This distinction is made based on the presence or absence of the Y chromosome, which carries genes related to male development.
The 23rd pair in a karyotype shows if it will be male or female
Homologous