nsv6104571
- Organism: Homo sapiens
- Study:nstd212 (Wu et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:73,522
- 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: 600 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 591 SVs from 65 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6104571 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000021.9 | Chr21 | 43,262,465 | 43,335,986 | ||
| nsv6104571 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 44,682,669 | 44,755,866 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17638796 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17638796 | Submitted genomic | NC_000021.9:g.4326 2465_43335986inv | GRCh38 (hg38) | NC_000021.9 | Chr21 | 43,262,465 | 43,335,986 | ||
| nssv17638796 | Remapped | Good | NC_000021.8:g.4468 2669_44755866inv | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 44,682,669 | 44,755,866 |