Using spin-polarized scanning tunneling microscopy we show that the magnetic order of 1 monolayer Mn on W(001) is a spin spiral propagating along h110i crystallographic directions. The spiral arises on the atomic scale with a period of about 2.2 nm, equivalent to only 10 atomic rows. Ab initio calculations identify the spin spiral as a left-handed cycloid stabilized by the Dzyaloshinskii-Moriya interaction, imposed by spin-orbit coupling, in the presence of softened ferromagnetic exchange coupling. Monte Carlo simulations explain the formation of a nanoscale labyrinth pattern, originating from the coexistence of the two possible rotational domains, that is intrinsic to the system. DOI: 10.1103/PhysRevLett.101.027201 PACS numbers: 75.70.Ak, 68.37.Ef, 71.15.Mb Magnetism-based data storage technology relies on the fact that information, i.e., the magnetic state of the area representing the bits, is stable over time. From the microscopic point of view, the direction of the magnetic moments is stabilized mainly by the spin-orbit interaction, which couples the spin to the crystal lattice and is responsible for the occurrence of easy and hard magnetization axes. Based on this picture, the need for nanoscale magnetic devices called scientists to the quest for high magnetic anisotropy materials (see, e.g., Ref.[1]).However, with decreasing magnetic bit sizes the structural inversion asymmetry of interfaces and surfaces comes into play. A surprising consequence of this fact was recently demonstrated [2], namely, that this symmetry breaking in combination with spin-orbit coupling (SOC) leads to the Dzyaloshinskii-Moriya interaction (DMI) favoring noncollinear magnetic order [3,4]. Although the DMI, because of its relativistic nature, is usually expected to be negligible compared to the nonrelativistic exchange interaction, it is sufficiently strong to impose a nanoscale leftrotating cycloidal spin spiral (SS) on the otherwise antiferromagnetic Mn monolayer on W(110): adjacent moments slightly deviate from the collinear configuration by about 7 , resulting in a long-period SS [2].Many open issues of this new phenomenon remain. In noncentrosymmetric bulk materials the DMI is the origin of the weak ferromagnetism of parent antiferromagnets [4]. What are the consequences of the DMI in thin films possessing ferromagnetic exchange coupling, e.g., can it destabilize a ferromagnetic state? And what happens to the long-range magnetic order if SS's of different propagation directions are energetically degenerate due to symmetry? Can the DMI modify the magnetic order even on the atomic scale?As shown in this Letter, 1 ML Mn=W 001 is an ideal system to address these points: As opposed to the antiferromagnetic Mn=W 110 , this system exhibits strong ferromagnetic exchange interaction [5] and a fourfoldsymmetric square surface lattice. Spin-polarized scanning tunneling microscopy (SP-STM) measurements reveal a SS, i.e., magnetic moments rotating continuously from one atom to the next, propagating along h110i directions with a period ...