esv1007968
- 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:11,156
- 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: 273 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 273 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 19 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1007968 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 1,928,703 | 1,939,858 |
| esv1007968 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 1,949,933 | 1,961,088 |
| esv1007968 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 1,906,509 | 1,917,664 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565351 | Remapped | Perfect | NC_000011.10:g.(19 28703_?)_(?_193985 8)ins17245 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 1,928,703 | 1,939,858 |
| essv3565351 | Remapped | Perfect | NC_000011.9:g.(194 9933_?)_(?_1961088 )ins17245 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 1,949,933 | 1,961,088 |
| essv3565351 | Submitted genomic | NC_000011.8:g.(190 6509_?)_(?_1917664 )ins17245 | NCBI36 (hg18) | NC_000011.8 | Chr11 | 1,906,509 | 1,917,664 |