esv1791695
- 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: 111 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 111 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 41 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1791695 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 76,414,693 | 76,414,693 |
| esv1791695 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 76,881,036 | 76,881,036 |
| esv1791695 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000014.7 | Chr14 | 75,950,789 | 75,950,789 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3830155 | Remapped | Perfect | NC_000014.9:g.7641 4693_76414694insA | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 76,414,693 | 76,414,693 |
| essv3830155 | Remapped | Perfect | NC_000014.8:g.7688 1036_76881037insA | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 76,881,036 | 76,881,036 |
| essv3830155 | Submitted genomic | NC_000014.7:g.7595 0789_75950790insA | NCBI36 (hg18) | NC_000014.7 | Chr14 | 75,950,789 | 75,950,789 |