esv1011295
- 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:17,994
- 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: 144 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 72 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1011295 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 50,332,837 | 50,350,830 |
| esv1011295 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 50,366,748 | 50,384,741 |
| esv1011295 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 48,924,249 | 48,942,242 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563989 | Remapped | Perfect | NC_000016.10:g.(50 332837_?)_(?_50350 830)inv17994 | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 50,332,837 | 50,350,830 |
| essv3563989 | Remapped | Perfect | NC_000016.9:g.(503 66748_?)_(?_503847 41)inv17994 | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 50,366,748 | 50,384,741 |
| essv3563989 | Submitted genomic | NC_000016.8:g.(489 24249_?)_(?_489422 42)inv17994 | NCBI36 (hg18) | NC_000016.8 | Chr16 | 48,924,249 | 48,942,242 |