esv991653
- 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:20,647
- 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: 353 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 359 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 179 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv991653 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 14,318,225 | 14,338,871 |
| esv991653 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 14,318,224 | 14,338,870 |
| esv991653 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 14,308,224 | 14,328,870 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565795 | Remapped | Perfect | NC_000009.12:g.(14 318225_?)_(?_14338 871)inv20647 | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 14,318,225 | 14,338,871 |
| essv3565795 | Remapped | Perfect | NC_000009.11:g.(14 318224_?)_(?_14338 870)inv20647 | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 14,318,224 | 14,338,870 |
| essv3565795 | Submitted genomic | NC_000009.10:g.(14 308224_?)_(?_14328 870)inv20647 | NCBI36 (hg18) | NC_000009.10 | Chr9 | 14,308,224 | 14,328,870 |