esv5192
- 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:1,855
- 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: 118 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 118 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 41 SVs from 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv5192 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 59,610,548 | 59,612,402 |
| esv5192 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 61,370,306 | 61,372,160 |
| esv5192 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 61,040,312 | 61,042,166 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv27633 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| essv27633 | Remapped | Perfect | NC_000010.11:g.(59 610548_?)_(?_59612 402)inv | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 59,610,548 | 59,612,402 |
| essv27633 | Remapped | Perfect | NC_000010.10:g.(61 370306_?)_(?_61372 160)inv | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 61,370,306 | 61,372,160 |
| essv27633 | Submitted genomic | NC_000010.9:g.(610 40312_?)_(?_610421 66)inv | NCBI36 (hg18) | NC_000010.9 | Chr10 | 61,040,312 | 61,042,166 |