nsv3168551
- Organism: Homo sapiens
- Study:nstd158 (Cleal et al. 2019)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:72,616,263
- Publication(s):Cleal et al. 2019
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: 209637 SVs from 151 studies. See in: genome view
Overlapping variant regions from other studies: 209309 SVs from 151 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3168551 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 7,798,337 (-310, +310) | 80,414,599 (-310, +310) |
| nsv3168551 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 7,798,570 (-310, +310) | 81,124,316 (-310, +310) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14239862 | inversion | DB51 | Sequencing | Paired-end mapping | 89 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14239862 | Remapped | Good | NC_000006.12:g.(77 98027_7798647)_(80 414289_80414909)in v206 | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 7,798,337 (-310, +310) | 80,414,599 (-310, +310) |
| nssv14239862 | Submitted genomic | NC_000006.11:g.(77 98260_7798880)_(81 124006_81124626)in v206 | GRCh37 (hg19) | NC_000006.11 | Chr6 | 7,798,570 (-310, +310) | 81,124,316 (-310, +310) |