esv1433285
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,927
- Publication(s):Levy et al. 2007
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: 308 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 309 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 18 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1433285 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 40,027,972 | 40,037,898 |
| esv1433285 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 41,399,899 | 41,409,825 |
| esv1433285 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000021.7 | Chr21 | 40,321,769 | 40,331,695 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4326251 | Remapped | Perfect | NC_000021.9:g.4002 7972_40037898inv | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 40,027,972 | 40,037,898 |
| essv4326251 | Remapped | Perfect | NC_000021.8:g.4139 9899_41409825inv | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 41,399,899 | 41,409,825 |
| essv4326251 | Submitted genomic | NC_000021.7:g.4032 1769_40331695inv | NCBI36 (hg18) | NC_000021.7 | Chr21 | 40,321,769 | 40,331,695 |