esv1939049
- 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: 291 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 291 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 172 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1939049 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 10,265,775 | 10,265,775 |
| esv1939049 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 10,265,887 | 10,265,887 |
| esv1939049 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 10,318,887 | 10,318,887 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4828870 | Remapped | Perfect | NC_000005.10:g.102 65775_10265776insT CTAT | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 10,265,775 | 10,265,775 |
| essv4828870 | Remapped | Perfect | NC_000005.9:g.1026 5887_10265888insTC TAT | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 10,265,887 | 10,265,887 |
| essv4828870 | Submitted genomic | NC_000005.8:g.1031 8887_10318888insTC TAT | NCBI36 (hg18) | NC_000005.8 | Chr5 | 10,318,887 | 10,318,887 |