nsv5663781
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Ebert et al. 2021
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: 131 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 131 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 | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5663781 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 47,115,716 | 47,115,716 | ||
| nsv5663781 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 47,149,627 | 47,149,627 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17080469 | insertion | SAMN00001695 | Sequencing | Sequence alignment | 6,153 |
| nssv17097247 | insertion | HG03371 | Sequencing | Sequence alignment | 2,852 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17080469 | Submitted genomic | NC_000016.10:g.471 15716_47115717ins6 3 | GRCh38 (hg38) | NC_000016.10 | Chr16 | 47,115,716 | 47,115,716 | ||
| nssv17097247 | Submitted genomic | NC_000016.10:g.471 15716_47115717ins1 78 | GRCh38 (hg38) | NC_000016.10 | Chr16 | 47,115,716 | 47,115,716 | ||
| nssv17080469 | Remapped | Perfect | NC_000016.9:g.4714 9627_47149628ins63 | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 47,149,627 | 47,149,627 |
| nssv17097247 | Remapped | Perfect | NC_000016.9:g.4714 9627_47149628ins17 8 | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 47,149,627 | 47,149,627 |