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Genetic variation can be identified at many levels. Identifying genetic variation is possible from observations of phenotypic variation in either quantitative traits (traits that vary continuously and are coded for by many genes, e.g., leg length in dogs) or discrete traits (traits that fall into discrete categories and are coded for by one or a few genes, e.g., white, pink, or red petal color ...
Examples of human phenotypic variability: people with different levels of skin colors, a normal distribution of IQ scores, the tallest recorded man in history - Robert Wadlow - with his father. Human variability, or human variation, is the range of possible values for any characteristic, physical or mental, of human beings.
A graphical representation of the typical human karyotype.. Genetic diversity is the total number of genetic characteristics in the genetic makeup of a species. It ranges widely, from the number of species to differences within species, and can be correlated to the span of survival for a species. [1]
Variation (astronomy), any perturbation of the mean motion or orbit of a planet or satellite, particularly of the moon; Genetic variation, the difference in DNA among individuals or the differences between populations Human genetic variation, genetic differences in and among populations of humans
In ecotypes, it is common for continuous, gradual geographic variation to impose analogous phenotypic and genetic variation, a situation which leads to the emergence of clines. [1] A well-known example of a cline is the skin color gradation in indigenous human populations worldwide, which is related to latitude and amounts of sunlight.
This variation rate is comparatively small compared to other species. For example, the effective population size of tigers which perhaps has the whole population size less than 10,000 in the wild is not much smaller than the human species indicating a much higher level of genetic diversity although they are close to extinction in the wild.
An acquired characteristic is a non-heritable change in a function or structure of a living organism caused after birth by disease, injury, accident, deliberate modification, variation, repeated use, disuse, misuse, or other environmental influence. Acquired traits are synonymous with acquired characteristics.
Genomic structural variation is the variation in structure of an organism's chromosome, such as deletions, duplications, copy-number variants, insertions, inversions and translocations. Originally, a structure variation affects a sequence length about 1kb to 3Mb, which is larger than SNPs and smaller than chromosome abnormality (though the ...