nsv1154303
- 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:180
- Description:Insertion of chr9:7742232-7741396
- 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: 436 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 437 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154303 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 21,437,407 | 21,437,586 |
| nsv1154303 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 21,455,525 | 21,455,704 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004171 | Remapped | Perfect | NC_000023.11:g.(21 437407_?)_(?_21437 586)ins836 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 21,437,407 | 21,437,586 |
| nssv4004171 | Submitted genomic | NC_000023.10:g.(21 455525_?)_(?_21455 704)ins836 | GRCh37 (hg19) | NC_000023.10 | ChrX | 21,455,525 | 21,455,704 |