nsv5851183
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,234
- 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: 253 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 53 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5851183 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 45,791,277 | 45,792,510 | ||
| nsv5851183 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871068.1 | Chr10|NW_0 03871068.1 | 62,392 | 63,625 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| nssv17459831 | copy number variation | Sequencing | Sequence alignment | 0 |
| nssv17466575 | copy number variation | Sequencing | Sequence alignment | 2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv17459831 | Submitted genomic | GRCh38 (hg38) | NC_000010.11 | Chr10 | 45,791,277 | 45,792,510 | ||
| nssv17466575 | Submitted genomic | GRCh38 (hg38) | NC_000010.11 | Chr10 | 45,791,277 | 45,792,510 | ||
| nssv17459831 | Remapped | Perfect | GRCh37.p13 | First Pass | NW_003871068.1 | Chr10|NW_0 03871068.1 | 62,392 | 63,625 |
| nssv17466575 | Remapped | Perfect | GRCh37.p13 | First Pass | NW_003871068.1 | Chr10|NW_0 03871068.1 | 62,392 | 63,625 |