The goal of this paper is to provide formulae for the expectation and variance of the height and length of the ancestral recombination graph (ARG). While the formula for the expectation of the height is known (see, e.g. Krone and Neuhauser (1997)), the other formulae seem to be new. We obtain in particular (see Theorem 4.1) a very simple formula which expresses the expectation of the length of the ARG as a linear combination of the expectations of both the length of the coalescent tree and the height of the ARG. Finally, we study the speed at which the ARG comes down from infinity.

In this paper exchangeable bisexual models with fixed population size and non-overlapping generations are introduced. Each generation consists of N pairs of individuals. The pairs of a generation have altogether 2N children. These individuals form randomly the N pairs of the next generation. The extinction probability of the descendants of a fixed number of pairs of generation 0 is discussed. Under suitable conditions it can be approximately described by the extinction probability of a Galton–Watson process, if the population size is large. Special examples are a bisexual Wright–Fisher model and models with a uniformly bounded number of children of a pair.

A general exchangeable model is introduced to study gene survival in populations whose size changes without density dependence. Necessary and sufficient conditions for the occurrence of fixation (that is the proportion of one of the types tending to 1 with probability 1) are obtained. These are then applied to the Wright–Fisher model, the Moran model, and conditioned branching-process models. For the Wright–Fisher model it is shown that certain fixation is equivalent to certain extinction of one of the types, but that this is not the case for the Moran model.

For the haploid genetic model of Moran, the joint distribution of the numbers of distinct ancestors of a collection of nested subsamples is derived. These results are shown to apply to the diffusion approximations of a wide variety of other genetic models, including the Wright–Fisher process. The results allow us to relate the ancestries of populations sampled at different times. Analogous results for a line-of-descent process that incorporates the effect of mutation are given. Some results about the ages of alleles in an infinite-alleles model are described.