esv2281059
- 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: 178 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 178 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 78 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2281059 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 93,151,463 | 93,151,463 |
| esv2281059 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 93,694,692 | 93,694,692 |
| esv2281059 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 91,495,696 | 91,495,696 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5001891 | Remapped | Perfect | NC_000015.10:g.931 51463_93151464insT | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 93,151,463 | 93,151,463 |
| essv5001891 | Remapped | Perfect | NC_000015.9:g.9369 4692_93694693insT | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 93,694,692 | 93,694,692 |
| essv5001891 | Submitted genomic | NC_000015.8:g.9149 5696_91495697insT | NCBI36 (hg18) | NC_000015.8 | Chr15 | 91,495,696 | 91,495,696 |