esv2421962
- Organism: Homo sapiens
- Study:estd195 (Altshuler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:39
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,251
- 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: 226 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 226 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 81 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2421962 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| esv2421962 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| esv2421962 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv5011345 | deletion | NA21723 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5015916 | deletion | NA18861 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5018470 | deletion | NA21418 | SNP array | SNP genotyping analysis | 1 | 141 |
| essv5026174 | deletion | NA19210 | SNP array | SNP genotyping analysis | 1 | 149 |
| essv5027851 | deletion | NA19102 | SNP array | SNP genotyping analysis | 1 | 141 |
| essv5032128 | deletion | NA19174 | SNP array | SNP genotyping analysis | 1 | 142 |
| essv5032744 | deletion | NA19679 | SNP array | SNP genotyping analysis | 1 | 125 |
| essv5036079 | deletion | NA18869 | SNP array | SNP genotyping analysis | 1 | 140 |
| essv5037372 | deletion | NA19118 | SNP array | SNP genotyping analysis | 1 | 127 |
| essv5037415 | deletion | NA19226 | SNP array | SNP genotyping analysis | 1 | 156 |
| essv5037940 | deletion | NA21339 | SNP array | SNP genotyping analysis | 1 | 143 |
| essv5046115 | deletion | NA21685 | SNP array | SNP genotyping analysis | 1 | 153 |
| essv5049552 | deletion | NA19248 | SNP array | SNP genotyping analysis | 1 | 145 |
| essv5049603 | deletion | NA21489 | SNP array | SNP genotyping analysis | 1 | 131 |
| essv5051861 | deletion | NA18871 | SNP array | SNP genotyping analysis | 1 | 151 |
| essv5053296 | deletion | NA19103 | SNP array | SNP genotyping analysis | 1 | 143 |
| essv5068262 | deletion | NA20348 | SNP array | SNP genotyping analysis | 1 | 167 |
| essv5071232 | deletion | NA18911 | SNP array | SNP genotyping analysis | 1 | 158 |
| essv5071502 | deletion | NA21636 | SNP array | SNP genotyping analysis | 1 | 134 |
| essv5077447 | deletion | NA21634 | SNP array | SNP genotyping analysis | 1 | 128 |
| essv5086707 | deletion | NA21451 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5093282 | deletion | NA20277 | SNP array | SNP genotyping analysis | 1 | 135 |
| essv5096853 | deletion | NA11894 | SNP array | SNP genotyping analysis | 1 | 122 |
| essv5102942 | deletion | NA18484 | SNP array | SNP genotyping analysis | 1 | 143 |
| essv5114140 | deletion | NA18863 | SNP array | SNP genotyping analysis | 1 | 149 |
| essv5123578 | deletion | NA18910 | SNP array | SNP genotyping analysis | 1 | 154 |
| essv5124037 | deletion | NA18486 | SNP array | SNP genotyping analysis | 1 | 158 |
| essv5127347 | deletion | NA19096 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5129129 | deletion | NA19176 | SNP array | SNP genotyping analysis | 1 | 162 |
| essv5129391 | deletion | NA19097 | SNP array | SNP genotyping analysis | 1 | 146 |
| essv5131200 | deletion | NA21365 | SNP array | SNP genotyping analysis | 1 | 129 |
| essv5134428 | deletion | NA21575 | SNP array | SNP genotyping analysis | 1 | 136 |
| essv5140814 | deletion | NA19440 | SNP array | SNP genotyping analysis | 1 | 131 |
| essv5141713 | deletion | NA18868 | SNP array | SNP genotyping analysis | 1 | 148 |
| essv5145552 | deletion | NA19982 | SNP array | SNP genotyping analysis | 1 | 139 |
| essv5147349 | deletion | NA21617 | SNP array | SNP genotyping analysis | 1 | 155 |
| essv5158028 | deletion | NA21366 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5158520 | deletion | NA19373 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5159923 | deletion | NA19651 | SNP array | SNP genotyping analysis | 1 | 156 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5011345 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5015916 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5018470 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5026174 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5027851 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5032128 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5032744 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5036079 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5037372 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5037415 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5037940 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5046115 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5049552 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5049603 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5051861 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5053296 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5068262 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5071232 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5071502 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5077447 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5086707 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5093282 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5096853 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5102942 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5114140 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5123578 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5124037 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5127347 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5129129 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5129391 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5131200 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5134428 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5140814 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5141713 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5145552 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5147349 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5158028 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5158520 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5159923 | Remapped | Perfect | NC_000018.10:g.(?_ 42351574)_(4235782 4_?)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 42,351,574 | 42,357,824 |
| essv5011345 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5015916 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5018470 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5026174 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5027851 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5032128 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5032744 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5036079 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5037372 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5037415 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5037940 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5046115 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5049552 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5049603 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5051861 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5053296 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5068262 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5071232 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5071502 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5077447 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5086707 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5093282 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5096853 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5102942 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5114140 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5123578 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5124037 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5127347 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5129129 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5129391 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5131200 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5134428 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5140814 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5141713 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5145552 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5147349 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5158028 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5158520 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5159923 | Remapped | Perfect | NC_000018.9:g.(?_3 9931539)_(39937789 _?)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 39,931,539 | 39,937,789 |
| essv5011345 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5015916 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5018470 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5026174 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5027851 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5032128 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5032744 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5036079 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5037372 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5037415 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5037940 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5046115 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5049552 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5049603 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5051861 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5053296 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5068262 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5071232 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5071502 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5077447 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5086707 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 | ||
| essv5093282 | Submitted genomic | NC_000018.8:g.(?_3 8185537)_(38191787 _?)del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 38,185,537 | 38,191,787 |