esv1791656
- 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: 219 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 219 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 121 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1791656 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 236,014,726 | 236,014,726 |
| esv1791656 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 236,923,370 | 236,923,370 |
| esv1791656 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 236,588,109 | 236,588,109 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3721116 | Remapped | Perfect | NC_000002.12:g.236 014726_236014727in sT | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 236,014,726 | 236,014,726 |
| essv3721116 | Remapped | Perfect | NC_000002.11:g.236 923370_236923371in sT | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 236,923,370 | 236,923,370 |
| essv3721116 | Submitted genomic | NC_000002.10:g.236 588109_236588110in sT | NCBI36 (hg18) | NC_000002.10 | Chr2 | 236,588,109 | 236,588,109 |