esv1010146
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:17,650
- Publication(s):Pang et al. 2010
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: 203 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 203 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 105 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1010146 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 96,273,501 | 96,291,150 |
| esv1010146 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 96,816,730 | 96,834,379 |
| esv1010146 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 94,617,734 | 94,635,383 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563551 | Remapped | Perfect | NC_000015.10:g.(96 273501_?)_(?_96291 150)inv17650 | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 96,273,501 | 96,291,150 |
| essv3563551 | Remapped | Perfect | NC_000015.9:g.(968 16730_?)_(?_968343 79)inv17650 | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 96,816,730 | 96,834,379 |
| essv3563551 | Submitted genomic | NC_000015.8:g.(946 17734_?)_(?_946353 83)inv17650 | NCBI36 (hg18) | NC_000015.8 | Chr15 | 94,617,734 | 94,635,383 |