esv3898
- Organism: Homo sapiens
- Study:estd3 (Wang et al. 2008)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:91
- Publication(s):Wang 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: 186 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 186 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 82 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3898 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 95,149,366 | 95,149,456 |
| esv3898 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 95,692,595 | 95,692,685 |
| esv3898 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 93,493,599 | 93,493,689 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv26339 | inversion | YH | Sequencing | Read depth and paired-end mapping | 2,682 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv26339 | Remapped | Perfect | NC_000015.10:g.(95 149366_?)_(?_95149 456)inv | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 95,149,366 | 95,149,456 |
| essv26339 | Remapped | Perfect | NC_000015.9:g.(956 92595_?)_(?_956926 85)inv | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 95,692,595 | 95,692,685 |
| essv26339 | Submitted genomic | NC_000015.8:g.(934 93599_?)_(?_934936 89)inv | NCBI36 (hg18) | NC_000015.8 | Chr15 | 93,493,599 | 93,493,689 |