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Table 3 Classification of identified structural variations

From: Sequence and analysis of a whole genome from Kuwaiti population subgroup of Persian ancestry

Type of structural variations Number in Persian Genome Reported in DGV Reported to overlap with repeat rich regions in rmsk
Deletions 7645 7190 (94.05%) 2969 (38.84%)
Duplications 1697 1575 (92.81%) 212 (12.49%)
Insertions 585 514 (87.86%) 362 (61.88%)
Inversions 135 104 (77.04%) 26 (19.26%)
Translocations 1076 900 (83.64%) 710 (65.98%)
  1. A detected structural variation is defined to be ‘known’ if at least 50% of the detected variation (e.g. deletion) overlaps with a known variation.