answersLogoWhite

0

No, it is normal for chromosomes to cross over. Crossing over is how we humans have genetic diversity.

User Avatar

Wiki User

14y ago

What else can I help you with?

Continue Learning about Biology

What is meant by chromosomal abnormality?

Chromosomal abnormality is a broader term, describing duplications, loss, gain etc, of a particular chromosome. More related to the structures in an ideogram.Genetic disorder is a much broader term that describes any chromosomal or genetic changes. A disease condition.


Is marfan syndrome a chromosomal abnormality?

No, Marfan syndrome is not a chromosomal abnormality. It is a genetic disorder caused by a mutation in the fibrillin-1 (FBN1) gene, which affects the body's connective tissue. This gene is located on chromosome 15.


The exchange of parts between non homologous chromosomes...?

is known as chromosomal translocation. This process can lead to genetic disorders if it disrupts the normal function of genes located on the chromosomes involved. Chromosomal translocations can be balanced, in which case they may have no noticeable effect, or unbalanced, which can result in various health issues.


Which type of chromosomal abnormalities is most likely to be viable in humans?

Trisomy 21 (Down syndrome) is the most common type of chromosomal abnormality that is viable in humans. Individuals with Down syndrome have an extra copy of chromosome 21, which can result in distinctive physical characteristics and developmental delays, but many individuals with Down syndrome lead healthy and fulfilling lives.


What is the longest phase in meiotic division?

The longest phase in meiotic division is prophase I. This phase involves significant chromosomal changes, including crossing over and genetic recombination, which contribute to genetic diversity. It is divided into subphases: leptotene, zygotene, pachytene, diplotene, and diakinesis.

Related Questions

If the disease is a chromosomal abnormality describe the abnormality?

what is the answer to this question


How can chromosomal abnormalities of an unborn baby be diagnosed during pregnancy?

By what is called as amniocentesis, you can diagnose the chromosomal abnormality of the unborn baby. You do this procedure under cover of ultrasonography. The fetal cells will give you complete picture of the chromosomal abnormality of the unborn child.


What is a chromosomal defect?

A abnormality in the size, shape, or number of chromosomes.


What type of condition is trisomy?

Trisomy an abnormality in chromosomal development.


What age is a mother is at greatest risk of having a child with a chromosomal abnormality?

A mother is at greatest risk of having a child with a chromosomal abnormality, such as Down syndrome, when she is over the age of 35. As women age, the quality of their eggs declines, increasing the likelihood of chromosomal errors during cell division. The risk continues to rise significantly with advancing maternal age, particularly after 40.


Is achondroplasia a chromosomal abnormality?

Yes, it takes place in chromosome 4.


Is anyone susceptible to this Down syndrome?

no, it is a chromosomal abnormality, not a contagious disease.


What is the number one cause of miscarriage?

chromosomal abnormality of the developing fetus.


What type of chromosomal abnormality is most likely to be viable in humans?

Trisomy


Abnormality that may be detected by examination of amniotic fluid?

substances or chromosomal abnormalities


Is chromosomal abnormality in albinism?

yes it is. It affects chromosome 11.


What is the medical term of trisomy 16?

It is called Patau syndrome and is a chromosomal abnormality