esv989719
- 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:21,864
- 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: 478 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 478 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 245 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv989719 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 150,400,089 | 150,421,952 |
| esv989719 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 149,568,358 | 149,590,226 |
| esv989719 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 149,319,016 | 149,340,884 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564836 | Remapped | Good | NC_000023.11:g.(15 0400089_?)_(?_1504 21952)inv21869 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 150,400,089 | 150,421,952 |
| essv3564836 | Remapped | Perfect | NC_000023.10:g.(14 9568358_?)_(?_1495 90226)inv21869 | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 149,568,358 | 149,590,226 |
| essv3564836 | Submitted genomic | NC_000023.9:g.(149 319016_?)_(?_14934 0884)inv21869 | NCBI36 (hg18) | NC_000023.9 | ChrX | 149,319,016 | 149,340,884 |