The invention discloses a gene detection library construction method and a kit for hereditary dilated cardiomyopathy, and relates to mutation of ANKRD1, BAG3, LDB3, LMNA, MYBPC3, MYH6, MYH7, RBM20, SCN5A, TCAP, TNNC1, TNNI3, TNNT2, TPM1 , TTN and VCL genes. Target regions include exon regions of coded amino acids of the 16 genes and 20 basic group regions of each of the upstream and downstream ofeach exon; in order to ensure the full coverage of the target regions, a target region liberty is acquired according to a hybridization probe capture method after library preparation and then amplified by the LMPCR (ligation mediated polymerase chain reaction) method, and a sample library for sequencing is acquired after library purification. The library construction method has the advantages thatthe steps are simple and fast, the library construction cost is reduced effectively, arrhythmia related genes are included, related gene mutations can be acquired quickly and accurately through an Illumina high-throughput sequencer, and accordingly, the library construction method is important for the hereditary dilated cardiomyopathy.