nsv513651
- Organism: Homo sapiens
- Study:nstd50 (Arlt et al. 2011)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:28,709
- Publication(s):Arlt et al. 2011
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: 249 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 249 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 66 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv513651 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 128,627,926 | 128,656,634 |
| nsv513651 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 128,346,769 | 128,375,477 |
| nsv513651 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 129,829,459 | 129,858,167 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv626903 | inversion | 1 | Sequencing | Paired-end mapping | 2,637 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv626903 | Remapped | Perfect | NC_000003.12:g.(12 8627926_?)_(?_1286 56634)inv28709 | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 128,627,926 | 128,656,634 |
| nssv626903 | Remapped | Perfect | NC_000003.11:g.(12 8346769_?)_(?_1283 75477)inv28709 | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 128,346,769 | 128,375,477 |
| nssv626903 | Submitted genomic | NC_000003.10:g.(12 9829459_?)_(?_1298 58167)inv28709 | NCBI36 (hg18) | NC_000003.10 | Chr3 | 129,829,459 | 129,858,167 |