esv2421297
- 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: 188 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 188 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 93 SVs from 10 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421297 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 123,560,075 | 123,560,075 |
| esv2421297 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 123,430,783 | 123,430,783 |
| esv2421297 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 122,935,993 | 122,935,993 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4793977 | Remapped | Perfect | NC_000011.10:g.123 560075_123560076in sG | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 123,560,075 | 123,560,075 |
| essv4793977 | Remapped | Perfect | NC_000011.9:g.1234 30783_123430784ins G | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 123,430,783 | 123,430,783 |
| essv4793977 | Submitted genomic | NC_000011.8:g.1229 35993_122935994ins G | NCBI36 (hg18) | NC_000011.8 | Chr11 | 122,935,993 | 122,935,993 |