esv1006962
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21,255
- Publication(s):Pang et al. 2010
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: 465 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 465 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 201 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1006962 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 46,951,137 | 46,972,391 |
| esv1006962 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 46,810,572 | 46,831,782 |
| esv1006962 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 46,695,516 | 46,716,726 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565437 | Remapped | Good | NC_000023.11:g.(46 951137_?)_(?_46972 391)inv21211 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 46,951,137 | 46,972,391 |
| essv3565437 | Remapped | Perfect | NC_000023.10:g.(46 810572_?)_(?_46831 782)inv21211 | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 46,810,572 | 46,831,782 |
| essv3565437 | Submitted genomic | NC_000023.9:g.(466 95516_?)_(?_467167 26)inv21211 | NCBI36 (hg18) | NC_000023.9 | ChrX | 46,695,516 | 46,716,726 |