Human Karyotyping Simulation SE - Exploration Activity Guide, Exams of Advanced Education

Human Karyotyping Simulation SE - Exploration Activity Guide

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2025/2026

Available from 04/08/2026

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Human Karyotyping Simulation SE - Exploration
Activity Guide
Student Exploration: Human Karyotyping
Directions: Follow the instructions to go through the simulation. Respond to the questions and
prompts in the orange boxes.
Vocabulary: autosome, chromosomal disorder, chromosome, genome, karyotype, sex chromosome
Prior Knowledge Question (Do this BEFORE using the Gizmo.)
A chromosome is a rod-shaped structure made of coils of DNA. Most human cells have 23 pairs of
chromosomes.
1. Why do you think humans have two sets of 23 chromosomes? (Hint: Where did each set come
from?)
2. How do you think different people’s chromosomes would compare?
Gizmo Warm-up
Scientists use karyotypes to study the chromosomes in a cell. A
karyotype is a picture showing a cell’s chromosomes grouped together
in pairs.
In the Human Karyotyping Gizmo, you will make karyotypes for five
individuals. Take a look at the SIMULATION pane. Use the arrows to click
through the numbered list of chromosomes at the bottom right of the
pane.
1. How does the appearance of the chromosomes change as
you move through the list?
2. Examine the chromosomes labeled x and y. How do these two
chromosomes compare?
You have two sets of chromosomes because you get one from each parent.
There would be different combinations in genes and different crossing over
options.
The chromosomes get smaller and smaller
The x chromosomes is much larger than the y chromosomes.
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Human Karyotyping Simulation SE - Exploration

Activity Guide

Student Exploration: Human Karyotyping

Directions: Follow the instructions to go through the simulation. Respond to the questions and prompts in the orange boxes. Vocabulary: autosome, chromosomal disorder, chromosome, genome, karyotype, sex chromosome

Prior Knowledge Question (Do this BEFORE using the Gizmo.)

A chromosome is a rod-shaped structure made of coils of DNA. Most human cells have 23 pairs of chromosomes.

  1. Why do you think humans have two sets of 23 chromosomes? (Hint: Where did each set come from?)
  2. How do you think different people’s chromosomes would compare? Gizmo Warm-up Scientists use karyotypes to study the chromosomes in a cell. A karyotype is a picture showing a cell’s chromosomes grouped together in pairs. In the Human Karyotyping Gizmo, you will make karyotypes for five individuals. Take a look at the SIMULATION pane. Use the arrows to click through the numbered list of chromosomes at the bottom right of the pane.
  3. How does the appearance of the chromosomes change as you move through the list?
  4. Examine the chromosomes labeled x and y. How do these two chromosomes compare? You have two sets of chromosomes because you get one from each parent. There would be different combinations in genes and different crossing over options. The chromosomes get smaller and smaller The x chromosomes is much larger than the y chromosomes.

Activity B: Chromosomal disorders Get the Gizmo ready: ● Click Reset. Question: How can you use a karyotype to diagnose a disease?

  1. Compare: Select Subject C from the SIMULATION pane. Identify each of subject C’s chromosomes, and place them on the KARYOTYPING pane. Once you have completed the karyotype, take a 📷 snapshot of it. Paste the 📷 snapshot into a document. Label it “Subject C.” How does subject C’s karyotype differ from a normal karyotype?
  2. Diagnose: A chromosomal disorder occurs when a person’s cells do not have the correct number of chromosomes. The table below lists three common chromosomal disorders. Disorder Description Subject Symptoms Down syndrom e Extra chromosome 21

E

Visual problems, hearing loss, speech problems,small head, and a small mouth Klinefelter syndrome Extra X in male (XXY)

C

Testicular changes in puberty Turner syndrom e Single X in female (XO)

D

Webbed neck, undeveloped ovaries, and diabetes Use the table to determine which disorder subject C has. Record your diagnosis in the third column of the table, and then click on the DIAGNOSIS tab to check your answer. Summarize the information on the DIAGNOSIS tab in the fourth column of the table. Extra X chromsome

  1. Generalize: Another chromosomal disorder, called Edward’s syndrome, occurs when a person’s cells have three copies of chromosome 18. People who have Edward’s syndrome have severe intellectual disabilities and their skeletons are malformed. Most people with Edward’s syndrome die in infancy. Use the above information about Edward’s syndrome and the descriptions of Down syndrome, Klinefelter syndrome, and Turner syndrome in the table on the previous page to compare these four different chromosomal disorders. A. Which type of chromosomal disorders seems to have the greatest affect on a person’s health—disorders involving autosomes or sex chromosomes? B. Why do you think this might be the case?
  2. Extend your thinking: Klinefelter syndrome only affects males, and Turner syndrome only affects females. Examine the karyotypes of the subjects you diagnosed with Klinefelter syndrome and Turner syndrome. A. How do you think sex is determined in a person with a chromosomal disorder involving the sex chromosomes? B. Individuals with a genetic disorder called trisomy X have three X chromosomes. (These individuals are normal and do not have any particular symptoms.) What sex would a person with trisomy X be?
  3. Summarize: The genome of an organism is its total genetic material. What aspects of the genome can and cannot be determined through karyotyping? Female Three copies of chromosome 18 There is disabilities and their skeletons are malformed, this is the cause of most people dying in infancy. You have to see if the three copies are on the X or Y chromosomes. Person’s trait and how severe the disorder can be