nsv5584081
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:16,791
- 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: 846 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 841 SVs from 82 studies. See in: genome view
Overlapping variant regions from other studies: 412 SVs from 38 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5584081 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 140,842,552 | 140,859,342 | ||
| nsv5584081 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000005.9 | Chr5 | 140,222,137 | 140,238,927 |
| nsv5584081 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_004775428.1 | Chr5|NW_00 4775428.1 | 77,728 | 94,518 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17123437 | Submitted genomic | NC_000005.10:g.140 842552_140859342de lA | GRCh38 (hg38) | NC_000005.10 | Chr5 | 140,842,552 | 140,859,342 | ||
| nssv17123437 | Remapped | Perfect | NW_004775428.1:g.7 7728_94518delA | GRCh37.p13 | First Pass | NW_004775428.1 | Chr5|NW_00 4775428.1 | 77,728 | 94,518 |
| nssv17123437 | Remapped | Perfect | NC_000005.9:g.1402 22137_140238927del A | GRCh37.p13 | Second Pass | NC_000005.9 | Chr5 | 140,222,137 | 140,238,927 |