nsv1154307
- 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:391
- Description:Insertion of chrM:12219-12168
- 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: 168 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 168 SVs from 32 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154307 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 6,247,150 | 6,247,540 |
| nsv1154307 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 6,356,316 | 6,356,706 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004177 | Remapped | Perfect | NC_000012.12:g.(62 47150_?)_(?_624754 0)ins51 | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 6,247,150 | 6,247,540 |
| nssv4004177 | Submitted genomic | NC_000012.11:g.(63 56316_?)_(?_635670 6)ins51 | GRCh37 (hg19) | NC_000012.11 | Chr12 | 6,356,316 | 6,356,706 |