nsv5865549
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,789
- Publication(s):Almarri et al. 2020
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: 207 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 206 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 31 SVs from 17 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5865549 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 133,217,241 | 133,227,029 | ||
| nsv5865549 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000009.11 | Chr9 | 136,092,628 | 136,102,416 |
| nsv5865549 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003315925.1 | Chr9|NW_00 3315925.1 | 43,187 | 52,975 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| nssv17511659 | copy number variation | Sequencing | Sequence alignment | 2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv17511659 | Submitted genomic | GRCh38 (hg38) | NC_000009.12 | Chr9 | 133,217,241 | 133,227,029 | ||
| nssv17511659 | Remapped | Perfect | GRCh37.p13 | First Pass | NW_003315925.1 | Chr9|NW_00 3315925.1 | 43,187 | 52,975 |
| nssv17511659 | Remapped | Perfect | GRCh37.p13 | Second Pass | NC_000009.11 | Chr9 | 136,092,628 | 136,102,416 |