esv1003613
- 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:42,755
- 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: 331 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 344 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 80 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1003613 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 152,261,602 | 152,304,356 |
| esv1003613 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 152,234,078 | 152,276,832 |
| esv1003613 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 150,500,702 | 150,543,456 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563823 | Remapped | Perfect | NC_000001.11:g.(15 2261602_?)_(?_1523 04356)inv42755 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 152,261,602 | 152,304,356 |
| essv3563823 | Remapped | Perfect | NC_000001.10:g.(15 2234078_?)_(?_1522 76832)inv42755 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 152,234,078 | 152,276,832 |
| essv3563823 | Submitted genomic | NC_000001.9:g.(150 500702_?)_(?_15054 3456)inv42755 | NCBI36 (hg18) | NC_000001.9 | Chr1 | 150,500,702 | 150,543,456 |