esv2421324
- 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: 127 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 127 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 33 SVs from 12 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421324 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 20,953,397 | 20,953,397 |
| esv2421324 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 20,994,889 | 20,994,889 |
| esv2421324 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 20,969,893 | 20,969,893 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4936289 | Remapped | Perfect | NC_000003.12:g.209 53397_20953398insT | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 20,953,397 | 20,953,397 |
| essv4936289 | Remapped | Perfect | NC_000003.11:g.209 94889_20994890insT | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 20,994,889 | 20,994,889 |
| essv4936289 | Submitted genomic | NC_000003.10:g.209 69893_20969894insT | NCBI36 (hg18) | NC_000003.10 | Chr3 | 20,969,893 | 20,969,893 |