esv1002951
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:19,708
- Publication(s):Pang 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: 792 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 792 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 497 SVs from 28 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1002951 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 76,589,731 | 76,609,438 |
| esv1002951 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 76,882,072 | 76,901,779 |
| esv1002951 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 74,669,127 | 74,688,834 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563889 | Remapped | Perfect | NC_000015.10:g.(76 589731_?)_(?_76609 438)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 76,589,731 | 76,609,438 |
| essv3563889 | Remapped | Perfect | NC_000015.9:g.(768 82072_?)_(?_769017 79)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 76,882,072 | 76,901,779 |
| essv3563889 | Submitted genomic | NC_000015.8:g.(746 69127_?)_(?_746888 34)del12152 | NCBI36 (hg18) | NC_000015.8 | Chr15 | 74,669,127 | 74,688,834 |