esv2421289
- 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: 117 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 117 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 44 SVs from 10 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421289 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 81,648,272 | 81,648,272 |
| esv2421289 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 84,263,187 | 84,263,187 |
| esv2421289 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 83,453,007 | 83,453,007 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4663540 | Remapped | Perfect | NC_000009.12:g.816 48272_81648273insA A | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 81,648,272 | 81,648,272 |
| essv4663540 | Remapped | Perfect | NC_000009.11:g.842 63187_84263188insA A | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 84,263,187 | 84,263,187 |
| essv4663540 | Submitted genomic | NC_000009.10:g.834 53007_83453008insA A | NCBI36 (hg18) | NC_000009.10 | Chr9 | 83,453,007 | 83,453,007 |