nstd195 | nssv16237266 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 881655 | | | 881655 | | Remapped | 1 |
nstd195 | nssv16237384 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 887171 | | | 890871 | | Remapped | 1 |
nstd195 | nssv16238971 | | copy number variation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 631921 | | | 634871 | | Remapped | 1 |
nstd195 | nssv16238972 | | copy number variation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 656371 | | | 657171 | | Remapped | 1 |
nstd195 | nssv16238973 | | deletion | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 734470 | | | 734471 | | Remapped | 1 |
nstd195 | nssv16238974 | | deletion | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 821304 | | | 821305 | | Remapped | 1 |
nstd195 | nssv16238987 | | deletion | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1595572 | | | 1595573 | | Remapped | 1 |
nstd195 | nssv16239495 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 870175 | | | 870175 | | Remapped | 1 |
nstd195 | nssv16239496 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 870174 | | | 870174 | | Remapped | 1 |
nstd195 | nssv16239804 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 879881 | | | 879881 | | Remapped | 1 |
nstd195 | nssv16240000 | | copy number variation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1099021 | | | 1099871 | | Remapped | 1 |
nstd195 | nssv16240001 | | deletion | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1718349 | | | 1718350 | | Remapped | 1 |
nstd195 | nssv16240002 | | copy number variation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2652212 | | | 2656212 | | Remapped | 1 |
nstd195 | nssv16240003 | | deletion | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2655497 | | | 2655498 | | Remapped | 1 |
nstd195 | nssv16240211 | | deletion | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1718508 | | | 1718509 | | Remapped | 1 |
nstd195 | nssv16240611 | | deletion | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1718631 | | | 1718632 | | Remapped | 1 |
nstd195 | nssv16242310 | | tandem duplication | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2123964 | | | 2123965 | | Remapped | 1 |
nstd195 | nssv16242425 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 879882 | | | 879882 | | Remapped | 1 |
nstd195 | nssv16242456 | | deletion | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1934923 | | | 1934924 | | Remapped | 1 |
nstd195 | nssv16243228 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 604771 | | | 605871 | | Remapped | 1 |
nstd195 | nssv16243427 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2652262 | | | 2655212 | | Remapped | 1 |
nstd195 | nssv16243774 | | deletion | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2657926 | | | 2657927 | | Remapped | 1 |
nstd195 | nssv16243810 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2671512 | | | 2672412 | | Remapped | 1 |
nstd195 | nssv16244138 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 632271 | | | 634971 | | Remapped | 1 |
nstd195 | nssv16245297 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 628871 | | | 632221 | | Remapped | 1 |
nstd195 | nssv16245723 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 12801 | | | 17551 | | Remapped | 1 |
nstd195 | nssv16245724 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 19851 | | | 20551 | | Remapped | 1 |
nstd195 | nssv16245725 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 818603 | | | 818603 | | Remapped | 1 |
nstd195 | nssv16245726 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 861922 | | | 861922 | | Remapped | 1 |
nstd195 | nssv16245727 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 879881 | | | 879881 | | Remapped | 1 |
nstd195 | nssv16245729 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1099021 | | | 1099871 | | Remapped | 1 |
nstd195 | nssv16245730 | | tandem duplication | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1488770 | | | 1488771 | | Remapped | 1 |
nstd195 | nssv16245731 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1718631 | | | 1718632 | | Remapped | 1 |
nstd195 | nssv16245732 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2652262 | | | 2656312 | | Remapped | 1 |
nstd195 | nssv16245733 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2655792 | | | 2655793 | | Remapped | 1 |
nstd195 | nssv16245734 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2656962 | | | 2659062 | | Remapped | 1 |
nstd195 | nssv16245735 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2657910 | | | 2657911 | | Remapped | 1 |
nstd195 | nssv16246289 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 656371 | | | 657171 | | Remapped | 1 |
nstd195 | nssv16247822 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 84051 | | | 90151 | | Remapped | 1 |
nstd195 | nssv16247823 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 628921 | | | 635821 | | Remapped | 1 |
nstd195 | nssv16247824 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 656421 | | | 657121 | | Remapped | 1 |
nstd195 | nssv16247826 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 818603 | | | 818603 | | Remapped | 1 |
nstd195 | nssv16247827 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 820962 | | | 820963 | | Remapped | 1 |
nstd195 | nssv16247828 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 878821 | | | 882721 | | Remapped | 1 |
nstd195 | nssv16247829 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 879881 | | | 879881 | | Remapped | 1 |
nstd195 | nssv16247830 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 885271 | | | 890921 | | Remapped | 1 |
nstd195 | nssv16247831 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1530531 | | | 1530532 | | Remapped | 1 |
nstd195 | nssv16247832 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2121514 | | | 2121515 | | Remapped | 1 |
nstd195 | nssv16247833 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2652503 | | | 2652504 | | Remapped | 1 |
nstd195 | nssv16247835 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2656484 | | | 2656485 | | Remapped | 1 |
nstd195 | nssv16247836 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2657909 | | | 2657910 | | Remapped | 1 |
nstd195 | nssv16247837 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2659612 | | | 2660362 | | Remapped | 1 |
nstd195 | nssv16247838 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2671562 | | | 2672412 | | Remapped | 1 |
nstd195 | nssv16247981 | | deletion | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 790163 | | | 790164 | | Remapped | 1 |
nstd195 | nssv16248894 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 879721 | | | 882721 | | Remapped | 1 |
nstd195 | nssv16249132 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 879708 | | | 879708 | | Remapped | 1 |
nstd195 | nssv16249579 | | copy number variation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 265150 | | | 266700 | | Remapped | 1 |
nstd195 | nssv16249580 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 820940 | | | 820941 | | Remapped | 1 |
nstd195 | nssv16249581 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 831213 | | | 831214 | | Remapped | 1 |
nstd195 | nssv16249582 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 861922 | | | 861922 | | Remapped | 1 |
nstd195 | nssv16249583 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2121965 | | | 2121966 | | Remapped | 1 |
nstd195 | nssv16249584 | | deletion | | Sequencing | Paired-end mapping | No | B450 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2123768 | | | 2123769 | | Remapped | 1 |
nstd195 | nssv16250387 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 880003 | | | 880003 | | Remapped | 1 |
nstd195 | nssv16250519 | | deletion | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 820962 | | | 820963 | | Remapped | 1 |
nstd195 | nssv16232665 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 264500 | | | 266650 | | Remapped | 1 |
nstd195 | nssv16232686 | | copy number variation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 628821 | | | 635571 | | Remapped | 1 |
nstd195 | nssv16232687 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 790988 | | | 790989 | | Remapped | 1 |
nstd195 | nssv16232688 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 880404 | | | 880404 | | Remapped | 1 |
nstd195 | nssv16232689 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 880404 | | | 880404 | | Remapped | 1 |
nstd195 | nssv16232690 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1718355 | | | 1718356 | | Remapped | 1 |
nstd195 | nssv16232691 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2656526 | | | 2656527 | | Remapped | 1 |
nstd195 | nssv16232693 | | copy number variation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2659612 | | | 2660312 | | Remapped | 1 |
nstd195 | nssv16232978 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 880024 | | | 880024 | | Remapped | 1 |
nstd195 | nssv16232997 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 882771 | | | 887121 | | Remapped | 1 |
nstd195 | nssv16233376 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 790225 | | | 790226 | | Remapped | 1 |
nstd195 | nssv16233377 | | copy number variation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 879821 | | | 882671 | | Remapped | 1 |
nstd195 | nssv16233378 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 880003 | | | 880003 | | Remapped | 1 |
nstd195 | nssv16233379 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 885526 | | | 885526 | | Remapped | 1 |
nstd195 | nssv16233380 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 885526 | | | 885526 | | Remapped | 1 |
nstd195 | nssv16233381 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 886836 | | | 886836 | | Remapped | 1 |
nstd195 | nssv16233382 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1412475 | | | 1412476 | | Remapped | 1 |
nstd195 | nssv16233383 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1934923 | | | 1934924 | | Remapped | 1 |
nstd195 | nssv16233384 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2121680 | | | 2121681 | | Remapped | 1 |
nstd195 | nssv16233385 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2121698 | | | 2121699 | | Remapped | 1 |
nstd195 | nssv16233386 | | copy number variation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2652262 | | | 2656312 | | Remapped | 1 |
nstd195 | nssv16233387 | | copy number variation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2656962 | | | 2659062 | | Remapped | 1 |
nstd195 | nssv16233562 | | copy number variation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 887221 | | | 890871 | | Remapped | 1 |
nstd195 | nssv16233563 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1207339 | | | 1207340 | | Remapped | 1 |
nstd195 | nssv16233565 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1289837 | | | 1289838 | | Remapped | 1 |
nstd195 | nssv16233566 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1530531 | | | 1530532 | | Remapped | 1 |
nstd195 | nssv16233567 | | deletion | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 2118014 | | | 2118015 | | Remapped | 1 |
nstd195 | nssv16233595 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M456 | | | GRCh38.p12 | NC_000001.11 | 1 | | 886836 | | | 886836 | | Remapped | 1 |
nstd195 | nssv16234497 | | copy number variation | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1099021 | | | 1099921 | | Remapped | 1 |
nstd195 | nssv16235706 | | deletion | | Sequencing | Paired-end mapping | No | B381 | | | GRCh38.p12 | NC_000001.11 | 1 | | 1530531 | | | 1530532 | | Remapped | 1 |
nstd195 | nssv16236742 | | copy number variation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 629071 | | | 629771 | | Remapped | 1 |
nstd195 | nssv16236743 | | copy number variation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 879271 | | | 882721 | | Remapped | 1 |
nstd195 | nssv16236865 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 881741 | | | 881741 | | Remapped | 1 |
nstd195 | nssv16236866 | | interchromosomal translocation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 881740 | | | 881740 | | Remapped | 1 |
nstd195 | nssv16237167 | | copy number variation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 264550 | | | 266500 | | Remapped | 1 |
nstd195 | nssv16237168 | | copy number variation | | Sequencing | Paired-end mapping | No | M478 | | | GRCh38.p12 | NC_000001.11 | 1 | | 885171 | | | 890921 | | Remapped | 1 |