esv990912
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15,593
- 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: 422 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 422 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 210 SVs from 26 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv990912 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 57,209,891 | 57,225,483 |
| esv990912 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 58,122,450 | 58,138,042 |
| esv990912 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 58,285,004 | 58,300,596 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564834 | Remapped | Perfect | NC_000008.11:g.(57 209891_?)_(?_57225 483)ins15788 | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 57,209,891 | 57,225,483 |
| essv3564834 | Remapped | Perfect | NC_000008.10:g.(58 122450_?)_(?_58138 042)ins15788 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 58,122,450 | 58,138,042 |
| essv3564834 | Submitted genomic | NC_000008.9:g.(582 85004_?)_(?_583005 96)ins15788 | NCBI36 (hg18) | NC_000008.9 | Chr8 | 58,285,004 | 58,300,596 |