esv1007306
- 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:10,922
- 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: 131 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 131 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 37 SVs from 12 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1007306 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 138,406,631 | 138,417,552 |
| esv1007306 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 137,742,320 | 137,753,241 |
| esv1007306 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 137,770,219 | 137,781,140 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563822 | Remapped | Perfect | NC_000005.10:g.(13 8406631_?)_(?_1384 17552)ins20488 | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 138,406,631 | 138,417,552 |
| essv3563822 | Remapped | Perfect | NC_000005.9:g.(137 742320_?)_(?_13775 3241)ins20488 | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 137,742,320 | 137,753,241 |
| essv3563822 | Submitted genomic | NC_000005.8:g.(137 770219_?)_(?_13778 1140)ins20488 | NCBI36 (hg18) | NC_000005.8 | Chr5 | 137,770,219 | 137,781,140 |