esv2421268
- 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: 107 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 107 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2421268 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 30,396,624 | 30,396,624 |
| esv2421268 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000022.10 | Chr22 | 30,792,613 | 30,792,613 |
| esv2421268 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000022.9 | Chr22 | 29,122,613 | 29,122,613 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4922152 | Remapped | Perfect | NC_000022.11:g.303 96624_30396625insA | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 30,396,624 | 30,396,624 |
| essv4922152 | Remapped | Perfect | NC_000022.10:g.307 92613_30792614insA | GRCh37.p13 | First Pass | NC_000022.10 | Chr22 | 30,792,613 | 30,792,613 |
| essv4922152 | Submitted genomic | NC_000022.9:g.2912 2613_29122614insA | NCBI36 (hg18) | NC_000022.9 | Chr22 | 29,122,613 | 29,122,613 |