esv1791692
- 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: 157 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 157 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 53 SVs from 12 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1791692 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 29,781,123 | 29,781,123 |
| esv1791692 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 29,934,056 | 29,934,056 |
| esv1791692 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 29,825,323 | 29,825,323 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4280496 | Remapped | Perfect | NC_000012.12:g.297 81123_29781124insC GCACTAGAAGATGCAGTT TC | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 29,781,123 | 29,781,123 |
| essv4280496 | Remapped | Perfect | NC_000012.11:g.299 34056_29934057insC GCACTAGAAGATGCAGTT TC | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 29,934,056 | 29,934,056 |
| essv4280496 | Submitted genomic | NC_000012.10:g.298 25323_29825324insC GCACTAGAAGATGCAGTT TC | NCBI36 (hg18) | NC_000012.10 | Chr12 | 29,825,323 | 29,825,323 |