nsv1154319
- Organism: Homo sapiens
- Study:nstd105 (Onozawa et al. 2015)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:384
- Description:Insertion of chrM:8701-8720
- Publication(s):Onozawa et al. 2015
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: 103 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 103 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154319 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 27,051,704 | 27,052,087 |
| nsv1154319 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 27,447,666 | 27,448,049 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv4004194 | insertion | NA18526 | Sequencing | Sequence alignment | nssv4004056, nssv4004124, nssv4004132 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004194 | Remapped | Perfect | NC_000022.11:g.(27 051704_?)_(?_27052 087)ins19 | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 27,051,704 | 27,052,087 |
| nssv4004194 | Submitted genomic | NC_000022.10:g.(27 447666_?)_(?_27448 049)ins19 | GRCh37 (hg19) | NC_000022.10 | Chr22 | 27,447,666 | 27,448,049 |