esv2421263
- Organism: Homo sapiens
- Study:estd194 (Bentley et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Bentley et al. 2008
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: 103 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 103 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 26 SVs from 7 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421263 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 69,983,485 | 69,983,485 |
| esv2421263 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 70,275,824 | 70,275,824 |
| esv2421263 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 68,062,878 | 68,062,878 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4888428 | Remapped | Perfect | NC_000015.10:g.699 83485_69983486insG | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 69,983,485 | 69,983,485 |
| essv4888428 | Remapped | Perfect | NC_000015.9:g.7027 5824_70275825insG | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 70,275,824 | 70,275,824 |
| essv4888428 | Submitted genomic | NC_000015.8:g.6806 2878_68062879insG | NCBI36 (hg18) | NC_000015.8 | Chr15 | 68,062,878 | 68,062,878 |