I am using svim-asm to identify the SVs from haplotype-resovled human genomes. However, there are multiple records in the same position, with same length and genotype, a case showed as followed:
chr1 16565784 svim_asm.INS.259 C CT..CA . PASS SVTYPE=INS;END=16565784;SVLEN=1548 GT 1/1
chr1 16565784 svim_asm.INS.260 C CT..CA . PASS SVTYPE=INS;END=16565784;SVLEN=1580 GT 1/0
chr1 16565784 svim_asm.INS.261 C CT..CA . PASS SVTYPE=INS;END=16565784;SVLEN=6297 GT 1/1
chr1 16565784 svim_asm.INS.262 C CT...CA . PASS SVTYPE=INS;END=16565784;SVLEN=6297 GT 1/1
chr1 16565784 svim_asm.INS.263 C CT...CA . PASS SVTYPE=INS;END=16565784;SVLEN=10970 GT 0/1
chr1 16565784 svim_asm.INS.264 C CT...CA . PASS SVTYPE=INS;END=16565784;SVLEN=15719 GT 1/1
Could you explain that why it happened, and what should we do with this type SV. Thank you very much!
Hi,
I am using svim-asm to identify the SVs from haplotype-resovled human genomes. However, there are multiple records in the same position, with same length and genotype, a case showed as followed:
chr1 16565784 svim_asm.INS.259 C CT..CA . PASS SVTYPE=INS;END=16565784;SVLEN=1548 GT 1/1 chr1 16565784 svim_asm.INS.260 C CT..CA . PASS SVTYPE=INS;END=16565784;SVLEN=1580 GT 1/0 chr1 16565784 svim_asm.INS.261 C CT..CA . PASS SVTYPE=INS;END=16565784;SVLEN=6297 GT 1/1 chr1 16565784 svim_asm.INS.262 C CT...CA . PASS SVTYPE=INS;END=16565784;SVLEN=6297 GT 1/1 chr1 16565784 svim_asm.INS.263 C CT...CA . PASS SVTYPE=INS;END=16565784;SVLEN=10970 GT 0/1 chr1 16565784 svim_asm.INS.264 C CT...CA . PASS SVTYPE=INS;END=16565784;SVLEN=15719 GT 1/1
Could you explain that why it happened, and what should we do with this type SV. Thank you very much!