esv1791720
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Levy et al. 2007
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: 476 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 476 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 252 SVs from 19 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1791720 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 134,321,928 | 134,321,928 |
| esv1791720 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 134,191,822 | 134,191,822 |
| esv1791720 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 133,697,032 | 133,697,032 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3613552 | Remapped | Perfect | NC_000011.10:g.134 321928_134321929in sA | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 134,321,928 | 134,321,928 |
| essv3613552 | Remapped | Perfect | NC_000011.9:g.1341 91822_134191823ins A | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 134,191,822 | 134,191,822 |
| essv3613552 | Submitted genomic | NC_000011.8:g.1336 97032_133697033ins A | NCBI36 (hg18) | NC_000011.8 | Chr11 | 133,697,032 | 133,697,032 |