nsv6089211
- Organism: Homo sapiens
- Study:nstd212 (Wu et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Wu 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: 157 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 155 SVs from 25 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6089211 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000017.11 | Chr17 | 41,167,977 | 41,167,977 | ||
| nsv6089211 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 39,324,229 | 39,324,229 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17625887 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17625887 | Submitted genomic | NC_000017.11:g.411 67977_41167978ins1 01 | GRCh38 (hg38) | NC_000017.11 | Chr17 | 41,167,977 | 41,167,977 | ||
| nssv17625887 | Remapped | Perfect | NC_000017.10:g.393 24229_39324230ins1 01 | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 39,324,229 | 39,324,229 |