nsv1154156
- 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:189
- Description:Insertion of chr19:13246106-13246032
- 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: 257 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 262 SVs from 31 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154156 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 241,994,434 | 241,994,622 |
| nsv1154156 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 242,157,736 | 242,157,924 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004088 | Remapped | Perfect | NC_000001.11:g.(24 1994434_?)_(?_2419 94622)ins74 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 241,994,434 | 241,994,622 |
| nssv4004088 | Submitted genomic | NC_000001.10:g.(24 2157736_?)_(?_2421 57924)ins74 | GRCh37 (hg19) | NC_000001.10 | Chr1 | 242,157,736 | 242,157,924 |