esv998773
- 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:21,453
- 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: 334 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 335 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 184 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv998773 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 40,021,203 | 40,042,655 |
| esv998773 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 41,393,130 | 41,414,582 |
| esv998773 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000021.7 | Chr21 | 40,315,000 | 40,336,452 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564195 | Remapped | Perfect | NC_000021.9:g.(400 21203_?)_(?_400426 55)inv21453 | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 40,021,203 | 40,042,655 |
| essv3564195 | Remapped | Perfect | NC_000021.8:g.(413 93130_?)_(?_414145 82)inv21453 | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 41,393,130 | 41,414,582 |
| essv3564195 | Submitted genomic | NC_000021.7:g.(403 15000_?)_(?_403364 52)inv21453 | NCBI36 (hg18) | NC_000021.7 | Chr21 | 40,315,000 | 40,336,452 |