esv2421897
- Organism: Homo sapiens
- Study:estd195 (Altshuler et al. 2010)
- Variant Type:complex substitution
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:38
- Validation:Not tested
- Clinical Assertions: No
- Region Size:31,331
- Publication(s):International HapMap 3 Consortium et al. 2010
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: 570 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 570 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 195 SVs from 26 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421897 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| esv2421897 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| esv2421897 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv5003913 | deletion | NA18101 | SNP array | SNP genotyping analysis | 1 | 140 |
| essv5007898 | duplication | NA11882 | SNP array | SNP genotyping analysis | 3 | 140 |
| essv5015493 | duplication | NA18140 | SNP array | SNP genotyping analysis | 3 | 152 |
| essv5016340 | duplication | NA18138 | SNP array | SNP genotyping analysis | 3 | 134 |
| essv5017931 | deletion | NA18108 | SNP array | SNP genotyping analysis | 1 | 146 |
| essv5030031 | duplication | NA18954 | SNP array | SNP genotyping analysis | 3 | 137 |
| essv5036007 | deletion | NA18978 | SNP array | SNP genotyping analysis | 1 | 135 |
| essv5039889 | duplication | NA18133 | SNP array | SNP genotyping analysis | 3 | 118 |
| essv5040413 | duplication | NA18959 | SNP array | SNP genotyping analysis | 3 | 132 |
| essv5045892 | duplication | NA18510 | SNP array | SNP genotyping analysis | 3 | 141 |
| essv5048029 | duplication | NA19918 | SNP array | SNP genotyping analysis | 3 | 136 |
| essv5051815 | deletion | NA20894 | SNP array | SNP genotyping analysis | 1 | 135 |
| essv5056578 | duplication | NA19209 | SNP array | SNP genotyping analysis | 3 | 146 |
| essv5058178 | deletion | NA21105 | SNP array | SNP genotyping analysis | 1 | 119 |
| essv5071068 | duplication | NA18991 | SNP array | SNP genotyping analysis | 3 | 130 |
| essv5072455 | duplication | NA18122 | SNP array | SNP genotyping analysis | 3 | 115 |
| essv5079146 | duplication | NA18555 | SNP array | SNP genotyping analysis | 3 | 134 |
| essv5081072 | deletion | NA11839 | SNP array | SNP genotyping analysis | 1 | 126 |
| essv5083929 | deletion | NA18969 | SNP array | SNP genotyping analysis | 1 | 139 |
| essv5085747 | deletion | NA10854 | SNP array | SNP genotyping analysis | 1 | 130 |
| essv5086389 | deletion | NA19059 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5091408 | duplication | NA19238 | SNP array | SNP genotyping analysis | 3 | 154 |
| essv5093696 | duplication | NA20897 | SNP array | SNP genotyping analysis | 3 | 134 |
| essv5093697 | duplication | NA19063 | SNP array | SNP genotyping analysis | 3 | 135 |
| essv5101173 | deletion | NA21491 | SNP array | SNP genotyping analysis | 1 | 154 |
| essv5114905 | deletion | NA20126 | SNP array | SNP genotyping analysis | 1 | 147 |
| essv5115804 | duplication | NA18965 | SNP array | SNP genotyping analysis | 3 | 129 |
| essv5120905 | duplication | NA19211 | SNP array | SNP genotyping analysis | 3 | 143 |
| essv5125699 | duplication | NA21357 | SNP array | SNP genotyping analysis | 3 | 150 |
| essv5127771 | deletion | NA18970 | SNP array | SNP genotyping analysis | 1 | 122 |
| essv5130957 | deletion | NA21143 | SNP array | SNP genotyping analysis | 1 | 129 |
| essv5131035 | duplication | NA20859 | SNP array | SNP genotyping analysis | 3 | 126 |
| essv5143791 | duplication | NA20284 | SNP array | SNP genotyping analysis | 3 | 149 |
| essv5144803 | duplication | NA18136 | SNP array | SNP genotyping analysis | 3 | 130 |
| essv5151925 | duplication | NA18995 | SNP array | SNP genotyping analysis | 3 | 138 |
| essv5155224 | deletion | NA19081 | SNP array | SNP genotyping analysis | 1 | 127 |
| essv5155845 | duplication | NA18594 | SNP array | SNP genotyping analysis | 3 | 131 |
| essv5157491 | duplication | NA19240 | SNP array | SNP genotyping analysis | 3 | 155 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5003913 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5007898 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5015493 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5016340 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5017931 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5030031 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5036007 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5039889 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5040413 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5045892 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5048029 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5051815 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5056578 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5058178 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5071068 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5072455 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5079146 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5081072 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5083929 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5085747 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5086389 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5091408 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5093696 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5093697 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5101173 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5114905 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5115804 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5120905 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5125699 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5127771 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5130957 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5131035 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5143791 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5144803 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5151925 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5155224 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5155845 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5157491 | Remapped | Perfect | NC_000019.10:g.(?_ 52824306)_(5285563 6_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,824,306 | 52,855,636 |
| essv5003913 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5007898 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5015493 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5016340 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5017931 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5030031 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5036007 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5039889 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5040413 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5045892 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5048029 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5051815 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5056578 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5058178 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5071068 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5072455 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5079146 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5081072 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5083929 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5085747 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5086389 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5091408 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5093696 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5093697 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5101173 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5114905 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5115804 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5120905 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5125699 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5127771 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5130957 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5131035 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5143791 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5144803 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5151925 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5155224 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5155845 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5157491 | Remapped | Perfect | NC_000019.9:g.(?_5 3327559)_(53358889 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,327,559 | 53,358,889 |
| essv5003913 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5007898 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5015493 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5016340 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5017931 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5030031 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5036007 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5039889 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5040413 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5045892 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5048029 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5051815 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5056578 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5058178 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5071068 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5072455 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5079146 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5081072 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5083929 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5085747 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5086389 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5091408 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5093696 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 | ||
| essv5093697 | Submitted genomic | NC_000019.8:g.(?_5 8019371)_(58050701 _?)dup | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,019,371 | 58,050,701 |