Long Read Sequencing of Filaggrin identifies extensive copy number variation in the FLG repeat of exon 3 and detects rare loss of function variants

Long-read sequencing data of 192 humans from Belgium, Ireland and Rwanda. Sequences have been obtained by PCR amplification of the FLG gene. Alignments are based on the hg19 reference (GRCh37).

本数据集涵盖来自比利时、爱尔兰及卢旺达的192名人类个体的长读长测序（Long-read sequencing）数据。所有序列均通过FLG基因的聚合酶链式反应（Polymerase Chain Reaction，PCR）扩增得到。序列比对以hg19（GRCh37）参考基因组为基准。