esv2421344
- Organism: Homo sapiens
- Study:estd195 (Altshuler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:32
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,282
- 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: 273 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 273 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 114 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2421344 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| esv2421344 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| esv2421344 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv5012463 | deletion | NA20907 | SNP array | SNP genotyping analysis | 1 | 129 |
| essv5015753 | deletion | NA12273 | SNP array | SNP genotyping analysis | 1 | 142 |
| essv5018431 | deletion | NA19770 | SNP array | SNP genotyping analysis | 1 | 126 |
| essv5030075 | deletion | NA19761 | SNP array | SNP genotyping analysis | 1 | 131 |
| essv5031884 | deletion | NA20828 | SNP array | SNP genotyping analysis | 1 | 136 |
| essv5034067 | deletion | NA20279 | SNP array | SNP genotyping analysis | 1 | 136 |
| essv5036978 | deletion | NA19773 | SNP array | SNP genotyping analysis | 1 | 133 |
| essv5041606 | deletion | NA12892 | SNP array | SNP genotyping analysis | 1 | 135 |
| essv5045328 | deletion | NA19678 | SNP array | SNP genotyping analysis | 1 | 139 |
| essv5049608 | deletion | NA20761 | SNP array | SNP genotyping analysis | 1 | 135 |
| essv5053000 | deletion | NA10846 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5063853 | deletion | NA12489 | SNP array | SNP genotyping analysis | 1 | 114 |
| essv5064339 | deletion | NA20803 | SNP array | SNP genotyping analysis | 1 | 131 |
| essv5064886 | deletion | NA21105 | SNP array | SNP genotyping analysis | 1 | 119 |
| essv5067251 | deletion | NA10850 | SNP array | SNP genotyping analysis | 1 | 118 |
| essv5071815 | deletion | NA20760 | SNP array | SNP genotyping analysis | 1 | 120 |
| essv5072618 | deletion | NA19759 | SNP array | SNP genotyping analysis | 1 | 124 |
| essv5075050 | deletion | NA11918 | SNP array | SNP genotyping analysis | 1 | 126 |
| essv5076216 | deletion | NA12145 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5078830 | deletion | NA20756 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5080339 | deletion | NA19651 | SNP array | SNP genotyping analysis | 1 | 156 |
| essv5083599 | deletion | NA20786 | SNP array | SNP genotyping analysis | 1 | 134 |
| essv5096583 | deletion | NA20845 | SNP array | SNP genotyping analysis | 1 | 127 |
| essv5102299 | deletion | NA19669 | SNP array | SNP genotyping analysis | 1 | 129 |
| essv5119331 | deletion | NA20765 | SNP array | SNP genotyping analysis | 1 | 140 |
| essv5119842 | deletion | NA20809 | SNP array | SNP genotyping analysis | 1 | 127 |
| essv5131398 | deletion | NA18158 | SNP array | SNP genotyping analysis | 1 | 128 |
| essv5133767 | deletion | NA20581 | SNP array | SNP genotyping analysis | 1 | 126 |
| essv5140051 | deletion | NA19676 | SNP array | SNP genotyping analysis | 1 | 134 |
| essv5147684 | deletion | NA12878 | SNP array | SNP genotyping analysis | 1 | 148 |
| essv5149109 | deletion | NA20586 | SNP array | SNP genotyping analysis | 1 | 141 |
| essv5157331 | deletion | NA20815 | SNP array | SNP genotyping analysis | 1 | 126 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5012463 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5015753 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5018431 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5030075 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5031884 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5034067 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5036978 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5041606 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5045328 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5049608 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5053000 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5063853 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5064339 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5064886 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5067251 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5071815 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5072618 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5075050 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5076216 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5078830 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5080339 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5083599 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5096583 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5102299 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5119331 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5119842 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5131398 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5133767 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5140051 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5147684 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5149109 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5157331 | Remapped | Perfect | NC_000002.12:g.(?_ 150174937)_(150181 218_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,174,937 | 150,181,218 |
| essv5012463 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5015753 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5018431 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5030075 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5031884 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5034067 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5036978 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5041606 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5045328 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5049608 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5053000 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5063853 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5064339 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5064886 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5067251 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5071815 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5072618 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5075050 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5076216 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5078830 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5080339 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5083599 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5096583 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5102299 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5119331 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5119842 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5131398 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5133767 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5140051 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5147684 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5149109 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5157331 | Remapped | Perfect | NC_000002.11:g.(?_ 151031451)_(151037 732_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,031,451 | 151,037,732 |
| essv5012463 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5015753 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5018431 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5030075 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5031884 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5034067 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5036978 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5041606 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5045328 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5049608 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5053000 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5063853 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5064339 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5064886 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5067251 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5071815 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5072618 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5075050 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5076216 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5078830 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5080339 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5083599 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5096583 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5102299 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5119331 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5119842 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5131398 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5133767 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5140051 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5147684 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5149109 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 | ||
| essv5157331 | Submitted genomic | NC_000002.10:g.(?_ 150739697)_(150745 978_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,739,697 | 150,745,978 |