esv2119730
- Organism: Homo sapiens
- Study:estd194 (Bentley et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Bentley 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: 138 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 138 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 36 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2119730 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 22,509,523 | 22,509,523 |
| esv2119730 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 22,511,146 | 22,511,146 |
| esv2119730 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 22,120,244 | 22,120,244 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4785372 | Remapped | Perfect | NC_000004.12:g.225 09523_22509524insA | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 22,509,523 | 22,509,523 |
| essv4785372 | Remapped | Perfect | NC_000004.11:g.225 11146_22511147insA | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 22,511,146 | 22,511,146 |
| essv4785372 | Submitted genomic | NC_000004.10:g.221 20244_22120245insA | NCBI36 (hg18) | NC_000004.10 | Chr4 | 22,120,244 | 22,120,244 |