nsv1154226
- 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:453
- Description:Insertion of chrM:10637-10673
- 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: 97 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 97 SVs from 24 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154226 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 103,767,522 | 103,767,974 |
| nsv1154226 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 105,527,280 | 105,527,732 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv4004172 | insertion | NA19026 | Sequencing | Sequence alignment | nssv4004068, nssv4004189 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004172 | Remapped | Perfect | NC_000010.11:g.(10 3767522_?)_(?_1037 67974)ins36 | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 103,767,522 | 103,767,974 |
| nssv4004172 | Submitted genomic | NC_000010.10:g.(10 5527280_?)_(?_1055 27732)ins36 | GRCh37 (hg19) | NC_000010.10 | Chr10 | 105,527,280 | 105,527,732 |