nsv1154313
- 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:418
- Description:Insertion of chrM:1736-1683
- 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: 150 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154313 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 48,638,303 | 48,638,720 |
| nsv1154313 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 46,715,665 | 46,716,082 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv4004183 | insertion | NA18956 | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004183 | Remapped | Perfect | NC_000017.11:g.(48 638303_?)_(?_48638 720)ins53 | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 48,638,303 | 48,638,720 |
| nssv4004183 | Submitted genomic | NC_000017.10:g.(46 715665_?)_(?_46716 082)ins53 | GRCh37 (hg19) | NC_000017.10 | Chr17 | 46,715,665 | 46,716,082 |