esv2421282
- 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: 229 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 229 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 84 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2421282 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 132,023,955 | 132,023,955 |
| esv2421282 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 133,036,202 | 133,036,202 |
| esv2421282 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 133,105,384 | 133,105,384 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4967320 | Remapped | Perfect | NC_000008.11:g.132 023955_132023956in sT | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 132,023,955 | 132,023,955 |
| essv4967320 | Remapped | Perfect | NC_000008.10:g.133 036202_133036203in sT | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 133,036,202 | 133,036,202 |
| essv4967320 | Submitted genomic | NC_000008.9:g.1331 05384_133105385ins T | NCBI36 (hg18) | NC_000008.9 | Chr8 | 133,105,384 | 133,105,384 |