esv1403387
- 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:1,930
- 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: 161 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 166 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 68 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1403387 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 227,493,838 | 227,495,767 |
| esv1403387 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 227,681,539 | 227,683,468 |
| esv1403387 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 225,748,162 | 225,750,091 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3625539 | Remapped | Perfect | NC_000001.11:g.227 493838_227495767in v | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 227,493,838 | 227,495,767 |
| essv3625539 | Remapped | Perfect | NC_000001.10:g.227 681539_227683468in v | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 227,681,539 | 227,683,468 |
| essv3625539 | Submitted genomic | NC_000001.9:g.2257 48162_225750091inv | NCBI36 (hg18) | NC_000001.9 | Chr1 | 225,748,162 | 225,750,091 |