esv3988629
- Organism: Homo sapiens
- Study:estd229 (Fakhro et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array, Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:42
- Validation:Not tested
- Clinical Assertions: No
- Region Size:14,428
- Publication(s):Fakhro et al. 2015
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1743 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 1211 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 1743 SVs from 70 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
esv3988629 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 1,523,013 | 1,537,440 |
esv3988629 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 205,384 | 219,811 |
esv3988629 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 1,526,785 | 1,541,212 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
essv25952582 | deletion | DGMQ-31639 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,641 |
essv26029203 | deletion | DGMQ-31274 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,454 |
essv25959562 | deletion | DGMQ-31711 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,479 |
essv25990837 | deletion | DGMQ-31449 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,630 |
essv26002976 | deletion | DGMQ-31444 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,542 |
essv26013751 | deletion | DGMQ-31245 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,474 |
essv26017202 | deletion | DGMQ-31714 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,443 |
essv26020647 | deletion | DGMQ-32302 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,531 |
essv25900897 | deletion | DGMQ-31607 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,655 |
essv25974884 | deletion | DGMQ-31623 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,664 |
essv26006426 | deletion | DGMQ-32121 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,702 |
essv25939539 | deletion | DGMQ-31131 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,468 |
essv26038028 | deletion | DGMQ-31725 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,478 |
essv25969711 | deletion | DGMQ-31123 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,704 |
essv25971584 | deletion | DGMQ-32118 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,534 |
essv25989147 | deletion | DGMQ-32148 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,526 |
essv25899148 | deletion | DGMQ-31625 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,558 |
essv25985706 | deletion | DGMQ-31508 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,545 |
essv25937887 | deletion | DGMQ-31029 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,562 |
essv25957789 | deletion | DGMQ-31433 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,606 |
essv25997793 | deletion | DGMQ-31568 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,594 |
essv25988567 | deletion | DGMQ-32182 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,451 |
essv26034351 | deletion | DGMQ-31606 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,677 |
essv26039687 | deletion | DGMQ-31516 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,622 |
essv25974885 | deletion | DGMQ-31623 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,664 |
essv25948592 | deletion | DGMQ-31105 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,808 |
essv25964621 | deletion | DGMQ-31617 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,636 |
essv26004633 | deletion | DGMQ-32064 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,555 |
essv25904440 | deletion | DGMQ-31237 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,475 |
essv26022307 | deletion | DGMQ-31724 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,583 |
essv25959563 | deletion | DGMQ-31711 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,479 |
essv25990838 | deletion | DGMQ-31449 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,630 |
essv25952583 | deletion | DGMQ-31639 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,641 |
essv25968127 | deletion | DGMQ-31705 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,442 |
essv25899150 | deletion | DGMQ-31625 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,558 |
essv25939622 | deletion | DGMQ-32293 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,587 |
essv26001313 | deletion | DGMQ-32250 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,486 |
essv25970267 | deletion | DGMQ-31513 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,620 |
essv25982095 | deletion | DGMQ-31614 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,654 |
essv25973299 | deletion | DGMQ-31416 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,428 |
essv25999581 | deletion | DGMQ-31125 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,569 |
essv26013752 | deletion | DGMQ-31245 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 1 | 1,474 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
essv25952582 | Remapped | Perfect | NT_187529.1:g.(205 384_?)_(?_208973)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 205,384 | 208,973 |
essv26029203 | Remapped | Perfect | NT_187529.1:g.(205 384_?)_(?_208973)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 205,384 | 208,973 |
essv25959562 | Remapped | Perfect | NT_187529.1:g.(206 540_?)_(?_211993)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 206,540 | 211,993 |
essv25990837 | Remapped | Perfect | NT_187529.1:g.(206 540_?)_(?_211993)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 206,540 | 211,993 |
essv26002976 | Remapped | Perfect | NT_187529.1:g.(206 540_?)_(?_211993)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 206,540 | 211,993 |
essv26013751 | Remapped | Perfect | NT_187529.1:g.(206 540_?)_(?_211993)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 206,540 | 211,993 |
essv26017202 | Remapped | Perfect | NT_187529.1:g.(206 540_?)_(?_211993)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 206,540 | 211,993 |
essv26020647 | Remapped | Perfect | NT_187529.1:g.(206 567_?)_(?_210178)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 206,567 | 210,178 |
essv25900897 | Remapped | Perfect | NT_187529.1:g.(207 362_?)_(?_212621)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 207,362 | 212,621 |
essv25974884 | Remapped | Perfect | NT_187529.1:g.(207 679_?)_(?_211119)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 207,679 | 211,119 |
essv26006426 | Remapped | Perfect | NT_187529.1:g.(207 679_?)_(?_211119)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 207,679 | 211,119 |
essv25939539 | Remapped | Perfect | NT_187529.1:g.(208 424_?)_(?_211979)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 208,424 | 211,979 |
essv26038028 | Remapped | Perfect | NT_187529.1:g.(208 424_?)_(?_211979)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 208,424 | 211,979 |
essv25969711 | Remapped | Perfect | NT_187529.1:g.(208 447_?)_(?_211557)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 208,447 | 211,557 |
essv25971584 | Remapped | Perfect | NT_187529.1:g.(208 856_?)_(?_211638)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 208,856 | 211,638 |
essv25989147 | Remapped | Perfect | NT_187529.1:g.(208 856_?)_(?_213442)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 208,856 | 213,442 |
essv25899148 | Remapped | Perfect | NT_187529.1:g.(208 856_?)_(?_213470)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 208,856 | 213,470 |
essv25985706 | Remapped | Perfect | NT_187529.1:g.(209 037_?)_(?_213687)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 209,037 | 213,687 |
essv25937887 | Remapped | Perfect | NT_187529.1:g.(210 106_?)_(?_217580)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 210,106 | 217,580 |
essv25957789 | Remapped | Perfect | NT_187529.1:g.(210 106_?)_(?_217580)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 210,106 | 217,580 |
essv25997793 | Remapped | Perfect | NT_187529.1:g.(210 106_?)_(?_217580)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 210,106 | 217,580 |
essv25988567 | Remapped | Perfect | NT_187529.1:g.(210 966_?)_(?_213445)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 210,966 | 213,445 |
essv26034351 | Remapped | Perfect | NT_187529.1:g.(211 062_?)_(?_215083)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 211,062 | 215,083 |
essv26039687 | Remapped | Perfect | NT_187529.1:g.(211 275_?)_(?_218080)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 211,275 | 218,080 |
essv25974885 | Remapped | Perfect | NT_187529.1:g.(211 426_?)_(?_216335)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 211,426 | 216,335 |
essv25948592 | Remapped | Perfect | NT_187529.1:g.(211 610_?)_(?_218079)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 211,610 | 218,079 |
essv25964621 | Remapped | Perfect | NT_187529.1:g.(212 550_?)_(?_215253)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 212,550 | 215,253 |
essv26004633 | Remapped | Perfect | NT_187529.1:g.(213 132_?)_(?_217196)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 213,132 | 217,196 |
essv25904440 | Remapped | Perfect | NT_187529.1:g.(213 388_?)_(?_217576)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 213,388 | 217,576 |
essv26022307 | Remapped | Perfect | NT_187529.1:g.(213 501_?)_(?_217059)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 213,501 | 217,059 |
essv25959563 | Remapped | Perfect | NT_187529.1:g.(214 227_?)_(?_217525)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 214,227 | 217,525 |
essv25990838 | Remapped | Perfect | NT_187529.1:g.(214 227_?)_(?_217525)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 214,227 | 217,525 |
essv25952583 | Remapped | Perfect | NT_187529.1:g.(214 803_?)_(?_217959)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 214,803 | 217,959 |
essv25968127 | Remapped | Perfect | NT_187529.1:g.(214 803_?)_(?_217959)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 214,803 | 217,959 |
essv25899150 | Remapped | Perfect | NT_187529.1:g.(214 839_?)_(?_219811)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 214,839 | 219,811 |
essv25939622 | Remapped | Perfect | NT_187529.1:g.(214 887_?)_(?_217563)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 214,887 | 217,563 |
essv26001313 | Remapped | Perfect | NT_187529.1:g.(214 887_?)_(?_217563)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 214,887 | 217,563 |
essv25970267 | Remapped | Perfect | NT_187529.1:g.(215 327_?)_(?_217582)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 215,327 | 217,582 |
essv25982095 | Remapped | Perfect | NT_187529.1:g.(215 350_?)_(?_218949)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 215,350 | 218,949 |
essv25973299 | Remapped | Perfect | NT_187529.1:g.(216 250_?)_(?_219018)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 216,250 | 219,018 |
essv25999581 | Remapped | Perfect | NT_187529.1:g.(216 250_?)_(?_219018)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 216,250 | 219,018 |
essv26013752 | Remapped | Perfect | NT_187529.1:g.(216 250_?)_(?_219018)d el | GRCh38.p12 | Second Pass | NT_187529.1 | Chr2|NT_18 7529.1 | 216,250 | 219,018 |
essv25952582 | Remapped | Perfect | NC_000002.12:g.(15 23013_?)_(?_152660 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,523,013 | 1,526,602 |
essv26029203 | Remapped | Perfect | NC_000002.12:g.(15 23013_?)_(?_152660 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,523,013 | 1,526,602 |
essv25959562 | Remapped | Perfect | NC_000002.12:g.(15 24169_?)_(?_152962 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,524,169 | 1,529,622 |
essv25990837 | Remapped | Perfect | NC_000002.12:g.(15 24169_?)_(?_152962 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,524,169 | 1,529,622 |
essv26002976 | Remapped | Perfect | NC_000002.12:g.(15 24169_?)_(?_152962 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,524,169 | 1,529,622 |
essv26013751 | Remapped | Perfect | NC_000002.12:g.(15 24169_?)_(?_152962 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,524,169 | 1,529,622 |
essv26017202 | Remapped | Perfect | NC_000002.12:g.(15 24169_?)_(?_152962 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,524,169 | 1,529,622 |
essv26020647 | Remapped | Perfect | NC_000002.12:g.(15 24196_?)_(?_152780 7)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,524,196 | 1,527,807 |
essv25900897 | Remapped | Perfect | NC_000002.12:g.(15 24991_?)_(?_153025 0)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,524,991 | 1,530,250 |
essv25974884 | Remapped | Perfect | NC_000002.12:g.(15 25308_?)_(?_152874 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,525,308 | 1,528,748 |
essv26006426 | Remapped | Perfect | NC_000002.12:g.(15 25308_?)_(?_152874 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,525,308 | 1,528,748 |
essv25939539 | Remapped | Perfect | NC_000002.12:g.(15 26053_?)_(?_152960 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,526,053 | 1,529,608 |
essv26038028 | Remapped | Perfect | NC_000002.12:g.(15 26053_?)_(?_152960 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,526,053 | 1,529,608 |
essv25969711 | Remapped | Perfect | NC_000002.12:g.(15 26076_?)_(?_152918 6)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,526,076 | 1,529,186 |
essv25971584 | Remapped | Perfect | NC_000002.12:g.(15 26485_?)_(?_152926 7)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,526,485 | 1,529,267 |
essv25989147 | Remapped | Perfect | NC_000002.12:g.(15 26485_?)_(?_153107 1)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,526,485 | 1,531,071 |
essv25899148 | Remapped | Perfect | NC_000002.12:g.(15 26485_?)_(?_153109 9)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,526,485 | 1,531,099 |
essv25985706 | Remapped | Perfect | NC_000002.12:g.(15 26666_?)_(?_153131 6)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,526,666 | 1,531,316 |
essv25937887 | Remapped | Perfect | NC_000002.12:g.(15 27735_?)_(?_153520 9)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,527,735 | 1,535,209 |
essv25957789 | Remapped | Perfect | NC_000002.12:g.(15 27735_?)_(?_153520 9)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,527,735 | 1,535,209 |
essv25997793 | Remapped | Perfect | NC_000002.12:g.(15 27735_?)_(?_153520 9)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,527,735 | 1,535,209 |
essv25988567 | Remapped | Perfect | NC_000002.12:g.(15 28595_?)_(?_153107 4)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,528,595 | 1,531,074 |
essv26034351 | Remapped | Perfect | NC_000002.12:g.(15 28691_?)_(?_153271 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,528,691 | 1,532,712 |
essv26039687 | Remapped | Perfect | NC_000002.12:g.(15 28904_?)_(?_153570 9)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,528,904 | 1,535,709 |
essv25974885 | Remapped | Perfect | NC_000002.12:g.(15 29055_?)_(?_153396 4)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,529,055 | 1,533,964 |
essv25948592 | Remapped | Perfect | NC_000002.12:g.(15 29239_?)_(?_153570 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,529,239 | 1,535,708 |
essv25964621 | Remapped | Perfect | NC_000002.12:g.(15 30179_?)_(?_153288 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,530,179 | 1,532,882 |
essv26004633 | Remapped | Perfect | NC_000002.12:g.(15 30761_?)_(?_153482 5)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,530,761 | 1,534,825 |
essv25904440 | Remapped | Perfect | NC_000002.12:g.(15 31017_?)_(?_153520 5)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,531,017 | 1,535,205 |
essv26022307 | Remapped | Perfect | NC_000002.12:g.(15 31130_?)_(?_153468 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,531,130 | 1,534,688 |
essv25959563 | Remapped | Perfect | NC_000002.12:g.(15 31856_?)_(?_153515 4)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,531,856 | 1,535,154 |
essv25990838 | Remapped | Perfect | NC_000002.12:g.(15 31856_?)_(?_153515 4)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,531,856 | 1,535,154 |
essv25952583 | Remapped | Perfect | NC_000002.12:g.(15 32432_?)_(?_153558 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,532,432 | 1,535,588 |
essv25968127 | Remapped | Perfect | NC_000002.12:g.(15 32432_?)_(?_153558 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,532,432 | 1,535,588 |
essv25899150 | Remapped | Perfect | NC_000002.12:g.(15 32468_?)_(?_153744 0)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,532,468 | 1,537,440 |
essv25939622 | Remapped | Perfect | NC_000002.12:g.(15 32516_?)_(?_153519 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,532,516 | 1,535,192 |
essv26001313 | Remapped | Perfect | NC_000002.12:g.(15 32516_?)_(?_153519 2)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,532,516 | 1,535,192 |
essv25970267 | Remapped | Perfect | NC_000002.12:g.(15 32956_?)_(?_153521 1)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,532,956 | 1,535,211 |
essv25982095 | Remapped | Perfect | NC_000002.12:g.(15 32979_?)_(?_153657 8)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,532,979 | 1,536,578 |
essv25973299 | Remapped | Perfect | NC_000002.12:g.(15 33879_?)_(?_153664 7)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,533,879 | 1,536,647 |
essv25999581 | Remapped | Perfect | NC_000002.12:g.(15 33879_?)_(?_153664 7)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,533,879 | 1,536,647 |
essv26013752 | Remapped | Perfect | NC_000002.12:g.(15 33879_?)_(?_153664 7)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 1,533,879 | 1,536,647 |
essv25952582 | Submitted genomic | NC_000002.11:g.(15 26785_?)_(?_153037 4)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,526,785 | 1,530,374 | ||
essv26029203 | Submitted genomic | NC_000002.11:g.(15 26785_?)_(?_153037 4)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,526,785 | 1,530,374 | ||
essv25959562 | Submitted genomic | NC_000002.11:g.(15 27941_?)_(?_153339 4)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,527,941 | 1,533,394 | ||
essv25990837 | Submitted genomic | NC_000002.11:g.(15 27941_?)_(?_153339 4)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,527,941 | 1,533,394 | ||
essv26002976 | Submitted genomic | NC_000002.11:g.(15 27941_?)_(?_153339 4)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,527,941 | 1,533,394 | ||
essv26013751 | Submitted genomic | NC_000002.11:g.(15 27941_?)_(?_153339 4)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,527,941 | 1,533,394 | ||
essv26017202 | Submitted genomic | NC_000002.11:g.(15 27941_?)_(?_153339 4)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,527,941 | 1,533,394 | ||
essv26020647 | Submitted genomic | NC_000002.11:g.(15 27968_?)_(?_153157 9)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,527,968 | 1,531,579 | ||
essv25900897 | Submitted genomic | NC_000002.11:g.(15 28763_?)_(?_153402 2)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,528,763 | 1,534,022 | ||
essv25974884 | Submitted genomic | NC_000002.11:g.(15 29080_?)_(?_153252 0)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,529,080 | 1,532,520 | ||
essv26006426 | Submitted genomic | NC_000002.11:g.(15 29080_?)_(?_153252 0)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,529,080 | 1,532,520 | ||
essv25939539 | Submitted genomic | NC_000002.11:g.(15 29825_?)_(?_153338 0)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,529,825 | 1,533,380 | ||
essv26038028 | Submitted genomic | NC_000002.11:g.(15 29825_?)_(?_153338 0)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,529,825 | 1,533,380 | ||
essv25969711 | Submitted genomic | NC_000002.11:g.(15 29848_?)_(?_153295 8)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,529,848 | 1,532,958 | ||
essv25971584 | Submitted genomic | NC_000002.11:g.(15 30257_?)_(?_153303 9)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,530,257 | 1,533,039 | ||
essv25989147 | Submitted genomic | NC_000002.11:g.(15 30257_?)_(?_153484 3)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 1,530,257 | 1,534,843 |