esv2421275
- 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: 153 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 153 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 55 SVs from 13 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421275 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 109,535,770 | 109,535,770 |
| esv2421275 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 108,871,471 | 108,871,471 |
| esv2421275 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 108,899,370 | 108,899,370 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4823007 | Remapped | Perfect | NC_000005.10:g.109 535770_109535771in sAGG | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 109,535,770 | 109,535,770 |
| essv4823007 | Remapped | Perfect | NC_000005.9:g.1088 71471_108871472ins AGG | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 108,871,471 | 108,871,471 |
| essv4823007 | Submitted genomic | NC_000005.8:g.1088 99370_108899371ins AGG | NCBI36 (hg18) | NC_000005.8 | Chr5 | 108,899,370 | 108,899,370 |