esv992424
- 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:18,959
- 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: 186 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 186 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 69 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv992424 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 80,448,801 | 80,467,759 |
| esv992424 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 80,842,581 | 80,861,538 |
| esv992424 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 79,366,712 | 79,385,669 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564913 | Remapped | Good | NC_000012.12:g.(80 448801_?)_(?_80467 759)inv18958 | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 80,448,801 | 80,467,759 |
| essv3564913 | Remapped | Perfect | NC_000012.11:g.(80 842581_?)_(?_80861 538)inv18958 | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 80,842,581 | 80,861,538 |
| essv3564913 | Submitted genomic | NC_000012.10:g.(79 366712_?)_(?_79385 669)inv18958 | NCBI36 (hg18) | NC_000012.10 | Chr12 | 79,366,712 | 79,385,669 |