esv1001997
- 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:27,024
- 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: 441 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 441 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 23 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1001997 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 1,915,600 | 1,942,623 |
| esv1001997 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 1,936,830 | 1,963,853 |
| esv1001997 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 1,893,406 | 1,920,429 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564032 | Remapped | Perfect | NC_000011.10:g.(19 15600_?)_(?_194262 3)inv27024 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 1,915,600 | 1,942,623 |
| essv3564032 | Remapped | Perfect | NC_000011.9:g.(193 6830_?)_(?_1963853 )inv27024 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 1,936,830 | 1,963,853 |
| essv3564032 | Submitted genomic | NC_000011.8:g.(189 3406_?)_(?_1920429 )inv27024 | NCBI36 (hg18) | NC_000011.8 | Chr11 | 1,893,406 | 1,920,429 |