esv1791675
- 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: 130 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 130 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 51 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1791675 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 124,983,802 | 124,983,802 |
| esv1791675 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 125,468,348 | 125,468,348 |
| esv1791675 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 124,034,301 | 124,034,301 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4150293 | Remapped | Perfect | NC_000012.12:g.124 983802_124983803in sA | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 124,983,802 | 124,983,802 |
| essv4150293 | Remapped | Perfect | NC_000012.11:g.125 468348_125468349in sA | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 125,468,348 | 125,468,348 |
| essv4150293 | Submitted genomic | NC_000012.10:g.124 034301_124034302in sA | NCBI36 (hg18) | NC_000012.10 | Chr12 | 124,034,301 | 124,034,301 |