esv1791667
- 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: 133 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 133 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 24 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1791667 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 101,160,254 | 101,160,254 |
| esv1791667 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 101,625,810 | 101,625,810 |
| esv1791667 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 101,398,398 | 101,398,398 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4047687 | Remapped | Perfect | NC_000001.11:g.101 160254_101160255in sA | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 101,160,254 | 101,160,254 |
| essv4047687 | Remapped | Perfect | NC_000001.10:g.101 625810_101625811in sA | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 101,625,810 | 101,625,810 |
| essv4047687 | Submitted genomic | NC_000001.9:g.1013 98398_101398399ins A | NCBI36 (hg18) | NC_000001.9 | Chr1 | 101,398,398 | 101,398,398 |