esv991598
- 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:18,194
- 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: 170 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 35 SVs from 13 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv991598 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 61,290,960 | 61,309,153 |
| esv991598 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 59,368,321 | 59,386,514 |
| esv991598 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 56,723,103 | 56,741,296 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565574 | Remapped | Perfect | NC_000017.11:g.(61 290960_?)_(?_61309 153)inv18194 | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 61,290,960 | 61,309,153 |
| essv3565574 | Remapped | Perfect | NC_000017.10:g.(59 368321_?)_(?_59386 514)inv18194 | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 59,368,321 | 59,386,514 |
| essv3565574 | Submitted genomic | NC_000017.9:g.(567 23103_?)_(?_567412 96)inv18194 | NCBI36 (hg18) | NC_000017.9 | Chr17 | 56,723,103 | 56,741,296 |