esv1791648
- 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: 119 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 23 SVs from 9 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1791648 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 86,329,574 | 86,329,574 |
| esv1791648 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 86,040,616 | 86,040,616 |
| esv1791648 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 85,718,264 | 85,718,264 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4041016 | Remapped | Perfect | NC_000011.10:g.863 29574_86329575insT T | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 86,329,574 | 86,329,574 |
| essv4041016 | Remapped | Perfect | NC_000011.9:g.8604 0616_86040617insTT | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 86,040,616 | 86,040,616 |
| essv4041016 | Submitted genomic | NC_000011.8:g.8571 8264_85718265insTT | NCBI36 (hg18) | NC_000011.8 | Chr11 | 85,718,264 | 85,718,264 |