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Sex determination

Reproduction and inheritance · Inheritance · note 6 of 6

Sex determinationSpec 3.26, 3.27

In short

Sex determination in humans depends on the sex chromosomes: females are XX and males are XY. Every egg carries an X chromosome, while half of the sperm carry an X and half carry a Y. So the sperm decides the sex of the baby at fertilisation, and there is a 50% probability of a boy or a girl.

Humans have 23 pairs of chromosomes. One pair is the sex chromosomes. Females have two X chromosomes (XX). Males have one X and one Y chromosome (XY).

All eggs carry an X chromosome. Half of the sperm carry an X and half carry a Y. The sex of the offspring is decided at fertilisation by which sperm fertilises the egg.

Genetic diagram for sex determination
X (egg)X (egg)
X (sperm)XX femaleXX female
Y (sperm)XY maleXY male

Two outcomes are female and two are male, so the ratio is 1 : 1 and there is a 50% probability that a baby will be a boy or a girl.

Common mistake:

The father's sperm decides the sex of the baby, because it carries either an X or a Y. Every egg carries an X.

Quick check

  1. What is an allele?

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    A different version (alternative form) of the same gene.

  2. What is the difference between genotype and phenotype?

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    Genotype is the alleles an organism has; phenotype is the characteristic that is expressed.

  3. What does homozygous mean?

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    Having two identical alleles of a gene.

  4. Two parents without a disorder have an affected child. Is the disorder dominant or recessive?

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    Recessive.

  5. Biology only What is codominance?

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    Both alleles are expressed in the phenotype of a heterozygous organism.

Written and checked against the Edexcel IGCSE Biology (4BI1) specification · Updated October 2026

Frequently asked questions

What is a genotype and phenotype?

A genotype is the alleles an organism has for a gene, written as letters such as TT, Tt or tt. A phenotype is the characteristic that is expressed and can be observed, such as tall or short. A heterozygous Tt plant has the dominant phenotype, because the dominant allele is expressed with only one copy.

What is a Punnett square used for in genetics?

A Punnett square is a genetic diagram used to show the possible offspring of a cross. The gametes from each parent are written along the top and side, then combined to give the offspring genotypes, phenotypes and ratios. For example, Tt × Tt gives 1 TT : 2 Tt : 1 tt, or 3 tall : 1 short.

How do you know if a characteristic is dominant or recessive from a family pedigree?

Find two parents with the same phenotype who have a child with the other phenotype. If two parents without the characteristic have an affected child, it is recessive and both parents are heterozygous carriers. If two parents with the characteristic have an unaffected child, it is dominant and both parents are heterozygous.

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