In the human karyotype, the 23 pairs of chromosomes are classified into 7 groups (A to G) based on their size and the position of the centromere. This classification is as follows:
1. Group A (Chromosomes 1–3): Largest chromosomes with metacentric or nearly metacentric centromeres.
2. Group B (Chromosomes 4–5): Large chromosomes with submetacentric centromeres.
3. Group C (Chromosomes 6–12, X): Medium-sized chromosomes with submetacentric centromeres.
4. Group D (Chromosomes 13–15): Medium-sized chromosomes with acrocentric centromeres and satellite structures.
5. Group E (Chromosomes 16–18): Small chromosomes with either metacentric (16) or submetacentric (17–18) centromeres.
6. Group F (Chromosomes 19–20): Small chromosomes with metacentric centromeres.
7. Group G (Chromosomes 21–22, Y): Smallest chromosomes with acrocentric centromeres; Y is unique due to its small size.
This grouping aids in identifying chromosomal abnormalities during cytogenetic analysis.
List I | List II |
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(A) Radiation hybrid mapping | (I) DNA can be cut into large fragments and circularized for use in chromosome walking |
(B) Sequence tagged site (STS) mapping | (II) Useful for cloning of overlapping DNA fragments (restricted to about 200 kb) |
(C) Chromosome jumping | (III) Fragment genome into large pieces and locate markers and genes |
(D) Chromosome walking | (IV) Applicable to any part of DNA sequence if some sequence information is available |