nsv5979143
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,718
- Description:DESC=[BREAKPOINT2]
- Publication(s):Almarri et al. 2020
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: 383 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 383 SVs from 50 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5979143 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000015.10 | Chr15 | 100,072,446 | 100,077,163 | ||
| nsv5979143 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 100,612,651 | 100,617,368 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17384248 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17384248 | Submitted genomic | NC_000015.10:g.100 072446_100077163in v | GRCh38 (hg38) | NC_000015.10 | Chr15 | 100,072,446 | 100,077,163 | ||
| nssv17384248 | Remapped | Perfect | NC_000015.9:g.1006 12651_100617368inv | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 100,612,651 | 100,617,368 |