The vacuum ultraviolet (VUV) laser pulsed field ionization photoelectron (PFI-PE) spectrum of cis-dichloroethene (cis-ClCH[Double Bond]CHCl) has been measured in the energy region of 77 600-79 500 cm(-1). On the basis of the semiempirical simulation of the origin PFI-PE band, we have obtained the IE(cis-ClCH[Double Bond]CHCl) to be 77 899.5+/-2.0 cm(-1) (9.658 39+/-0.000 25 eV). The assignment of the vibrational bands resolved in the VUV-PFI-PE spectrum are guided by high-level ab initio calculations of the vibrational frequencies for cis-ClCH[Double Bond]CHCl(+) and the Franck-Condon factors for the ionization transitions. Combining the results of the present VUV-PFI-PE measurement and the recent VUV-infrared-photoinduced Rydberg ionization study, the vibrational frequencies for eleven of the twelve vibrational modes of cis-ClCH[Double Bond]CHCl(+) have been experimentally determined: nu(1) (+)(a(1))=181 cm(-1), nu(2) (+)(a(2))=277 cm(-1), nu(3) (+)(b(2))=580 cm(-1), nu(4) (+)(b(1))=730 cm(-1), nu(5) (+)(a(1))=810 cm(-1), nu(6) (+)(a(2))=901 cm(-1), nu(8) (+)(a(1))=1196 cm(-1), nu(9) (+)(b(2))=1348 cm(-1), nu(10) (+)(a(1))=1429 cm(-1), nu(11) (+)(b(2))=3067 cm(-1), and nu(12) (+)(a(1))=3090 cm(-1)). These values are compared to theoretical anharmonic vibrational frequencies obtained at the MP2/6-311G(2df,p) and CCSD(T)/6-311G(2df,p) levels. The IE prediction for cis-ClCH[Double Bond]CHCl has also been calculated with the wave function based CCSD(T)/CBS method, which involves the approximation to the complete basis set (CBS) and the high-level correlation corrections. The theoretical IE(cis-ClCH[Double Bond]CHCl)=9.668 eV thus obtained is found to have a deviation of less than 10 meV with respect to the experimental IE value.