esv2421310
- 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: 182 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 182 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 74 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2421310 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 114,450,827 | 114,450,827 |
| esv2421310 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 117,213,107 | 117,213,107 |
| esv2421310 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 116,252,928 | 116,252,928 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4550316 | Remapped | Perfect | NC_000009.12:g.114 450827_114450828in sC | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 114,450,827 | 114,450,827 |
| essv4550316 | Remapped | Perfect | NC_000009.11:g.117 213107_117213108in sC | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 117,213,107 | 117,213,107 |
| essv4550316 | Submitted genomic | NC_000009.10:g.116 252928_116252929in sC | NCBI36 (hg18) | NC_000009.10 | Chr9 | 116,252,928 | 116,252,928 |