esv1765110
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,114
- 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: 282 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 282 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 18 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1765110 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 128,452,922 | 128,459,035 |
| esv1765110 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 129,465,168 | 129,471,281 |
| esv1765110 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 129,534,350 | 129,540,463 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3738853 | Remapped | Perfect | NC_000008.11:g.128 452922_128459035de l | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 128,452,922 | 128,459,035 |
| essv3738853 | Remapped | Perfect | NC_000008.10:g.129 465168_129471281de l | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 129,465,168 | 129,471,281 |
| essv3738853 | Submitted genomic | NC_000008.9:g.1295 34350_129540463del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 129,534,350 | 129,540,463 |