esv2421307
- 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: 217 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 217 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 81 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2421307 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 33,582,548 | 33,582,548 |
| esv2421307 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 31,162,512 | 31,162,512 |
| esv2421307 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000018.8 | Chr18 | 29,416,510 | 29,416,510 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4946783 | Remapped | Perfect | NC_000018.10:g.335 82548_33582549insT TTG | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 33,582,548 | 33,582,548 |
| essv4946783 | Remapped | Perfect | NC_000018.9:g.3116 2512_31162513insTT TG | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 31,162,512 | 31,162,512 |
| essv4946783 | Submitted genomic | NC_000018.8:g.2941 6510_29416511insTT TG | NCBI36 (hg18) | NC_000018.8 | Chr18 | 29,416,510 | 29,416,510 |