CNV(SO:0001019)

Loss(SO:0001743)

DGVa - Database of Genomic Variants Archive

nstd121 - Kader 2016 "The Copy Number Variation (CNV), as an essential form of genetic variation, has been increasingly recognized as one promising genetic marker in the analyses of animal genomes. Here we used the Equine 70K SNP genotyping array for the genome-wide detection of CNVs in 96 horses from three diverse Chinese breeds, Debao pony (DB), Mongolian (MG) and Yili (YL) horse. A total of 287 CNVs were determined and merged into 122 CNV regions (CNVRs) ranging from 199 bp to 2344 kb in size and distributed in a heterogeneous manner on chromosomes."

Chromosome 31:23869434-24195796 (forward strand) | View in location tab

326,363 bp

This structural variant overlaps 2 transcripts and is supported by 4 pieces of evidence.