nsv6046571
- 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: 131 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 135 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6046571 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 166,947,324 | 166,947,324 | ||
| nsv6046571 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 166,916,561 | 166,916,561 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17520689 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17520689 | Submitted genomic | NC_000001.11:g.166 947324_166947325in s306 | GRCh38 (hg38) | NC_000001.11 | Chr1 | 166,947,324 | 166,947,324 | ||
| nssv17520689 | Remapped | Perfect | NC_000001.10:g.166 916561_166916562in s306 | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 166,916,561 | 166,916,561 |