esv1791700
- 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: 94 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 94 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 34 SVs from 8 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1791700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 149,056,223 | 149,056,223 |
| esv1791700 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 149,377,359 | 149,377,359 |
| esv1791700 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 149,419,052 | 149,419,052 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4194841 | Remapped | Perfect | NC_000006.12:g.149 056223_149056224in sT | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 149,056,223 | 149,056,223 |
| essv4194841 | Remapped | Perfect | NC_000006.11:g.149 377359_149377360in sT | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 149,377,359 | 149,377,359 |
| essv4194841 | Submitted genomic | NC_000006.10:g.149 419052_149419053in sT | NCBI36 (hg18) | NC_000006.10 | Chr6 | 149,419,052 | 149,419,052 |