nsv1154306
- 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:332
- Description:Insertion of chrM:3809-3620
- 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: 148 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154306 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 121,130,907 | 121,131,238 |
| nsv1154306 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 121,001,616 | 121,001,947 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004176 | Remapped | Perfect | NC_000011.10:g.(12 1130907_?)_(?_1211 31238)ins189 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 121,130,907 | 121,131,238 |
| nssv4004176 | Submitted genomic | NC_000011.9:g.(121 001616_?)_(?_12100 1947)ins189 | GRCh37 (hg19) | NC_000011.9 | Chr11 | 121,001,616 | 121,001,947 |