esv1791654
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Levy et al. 2007
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: 122 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 39 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1791654 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 172,803,822 | 172,803,822 |
| esv1791654 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 172,521,612 | 172,521,612 |
| esv1791654 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 174,004,306 | 174,004,306 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4350208 | Remapped | Perfect | NC_000003.12:g.172 803822_172803823in sT | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 172,803,822 | 172,803,822 |
| essv4350208 | Remapped | Perfect | NC_000003.11:g.172 521612_172521613in sT | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 172,521,612 | 172,521,612 |
| essv4350208 | Submitted genomic | NC_000003.10:g.174 004306_174004307in sT | NCBI36 (hg18) | NC_000003.10 | Chr3 | 174,004,306 | 174,004,306 |