esv991505
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:18,027
- 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: 490 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 490 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 272 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv991505 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 46,363,996 | 46,382,022 |
| esv991505 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 47,783,911 | 47,801,937 |
| esv991505 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000021.7 | Chr21 | 46,608,339 | 46,626,365 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563608 | Remapped | Perfect | NC_000021.9:g.(463 63996_?)_(?_463820 22)inv18027 | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 46,363,996 | 46,382,022 |
| essv3563608 | Remapped | Perfect | NC_000021.8:g.(477 83911_?)_(?_478019 37)inv18027 | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 47,783,911 | 47,801,937 |
| essv3563608 | Submitted genomic | NC_000021.7:g.(466 08339_?)_(?_466263 65)inv18027 | NCBI36 (hg18) | NC_000021.7 | Chr21 | 46,608,339 | 46,626,365 |