esv1091998
- 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:5,671
- 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: 463 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 461 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 206 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1091998 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 49,157,285 | 49,162,955 |
| esv1091998 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 49,013,623 | 49,019,293 |
| esv1091998 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 48,900,567 | 48,906,237 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3970109 | Remapped | Perfect | NC_000023.11:g.491 57285_49162955inv | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 49,157,285 | 49,162,955 |
| essv3970109 | Remapped | Perfect | NC_000023.10:g.490 13623_49019293inv | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 49,013,623 | 49,019,293 |
| essv3970109 | Submitted genomic | NC_000023.9:g.4890 0567_48906237inv | NCBI36 (hg18) | NC_000023.9 | ChrX | 48,900,567 | 48,906,237 |