esv1001859
- 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:18,593
- 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: 161 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 161 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 59 SVs from 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1001859 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 123,976,462 | 123,995,054 |
| esv1001859 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 126,738,741 | 126,757,333 |
| esv1001859 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 125,778,562 | 125,797,154 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564048 | Remapped | Perfect | NC_000009.12:g.(12 3976462_?)_(?_1239 95054)inv18593 | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 123,976,462 | 123,995,054 |
| essv3564048 | Remapped | Perfect | NC_000009.11:g.(12 6738741_?)_(?_1267 57333)inv18593 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 126,738,741 | 126,757,333 |
| essv3564048 | Submitted genomic | NC_000009.10:g.(12 5778562_?)_(?_1257 97154)inv18593 | NCBI36 (hg18) | NC_000009.10 | Chr9 | 125,778,562 | 125,797,154 |