esv2421273
- 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: 125 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 41 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2421273 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 151,706,676 | 151,706,676 |
| esv2421273 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 152,627,828 | 152,627,828 |
| esv2421273 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 152,847,278 | 152,847,278 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4601407 | Remapped | Perfect | NC_000004.12:g.151 706676_151706677in sGC | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 151,706,676 | 151,706,676 |
| essv4601407 | Remapped | Perfect | NC_000004.11:g.152 627828_152627829in sGC | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 152,627,828 | 152,627,828 |
| essv4601407 | Submitted genomic | NC_000004.10:g.152 847278_152847279in sGC | NCBI36 (hg18) | NC_000004.10 | Chr4 | 152,847,278 | 152,847,278 |