nsv1154258
- 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:3,439
- Description:Insertion of chrM:6919-6951
- 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: 155 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 155 SVs from 36 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154258 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 53,778,838 | 53,782,276 |
| nsv1154258 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 54,244,511 | 54,247,949 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv4004188 | insertion | NA19020 | Sequencing | Sequence alignment | nssv4004158, nssv4004153, nssv4004135 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004188 | Remapped | Perfect | NC_000001.11:g.(53 778838_?)_(?_53782 276)ins32 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 53,778,838 | 53,782,276 |
| nssv4004188 | Submitted genomic | NC_000001.10:g.(54 244511_?)_(?_54247 949)ins32 | GRCh37 (hg19) | NC_000001.10 | Chr1 | 54,244,511 | 54,247,949 |