nsv1154302
- 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:31
- Description:Insertion of chr9:91093582-91091750
- 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: 245 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 245 SVs from 41 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154302 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 44,411,213 | 44,411,243 |
| nsv1154302 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 44,880,416 | 44,880,446 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv4004202 | insertion | NA19017 | Sequencing | Sequence alignment | nssv4004073, nssv4004138 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004202 | Remapped | Perfect | NC_000014.9:g.(444 11213_?)_(?_444112 43)ins1832 | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 44,411,213 | 44,411,243 |
| nssv4004202 | Submitted genomic | NC_000014.8:g.(448 80416_?)_(?_448804 46)ins1832 | GRCh37 (hg19) | NC_000014.8 | Chr14 | 44,880,416 | 44,880,446 |