Alternate interactions between the H19 imprinting control region (ICR) and one of the two Igf2 differentially methylated regions (DMR) has been proposed as a model regulating the reciprocal imprinting of Igf2 and H19. To study the conformation of this "imprint switch," we performed a systematic structural analysis across the 140 Kb of the mouse Igf2-H19 region, which includes enhancers located both between the two genes as well as downstream of H19, by using a scanning chromosome conformation capture (3C) technique. Our results suggest that on the active paternal Igf2 allele, the various enhancers have direct access to the Igf2 promoters, while the imprinted silent maternal Igf2 allele assumes a complex three-dimensional "knotted loop" that keeps the enhancers away from the Igf2 promoters and allows them to interact with the H19 promoter. This complex DNA looping of the maternal allele is formed by interactions involving DMR1, the ICR, and enhancers. Binding of CTCF to the maternal, unmethylated ICR in conjunction with the presence of multi-complex components, including interchromosomal interactions, creates a barrier blocking the access of all enhancers to Igf2, thereby silencing the maternal Igf2. This silencing configuration exists in newborn liver, mouse embryonic fibroblast (MEF), and embryonic stem (ES) cells and persists during mitosis, conferring a mechanism for epigenetic memory.