nsv5947158
- 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:64,997
- 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: 2356 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 2392 SVs from 91 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5947158 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000014.9 | Chr14 | 105,646,452 | 105,711,448 | ||
| nsv5947158 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 106,112,789 | 106,177,785 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17377818 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17377818 | Submitted genomic | NC_000014.9:g.1056 46452_105711448del | GRCh38 (hg38) | NC_000014.9 | Chr14 | 105,646,452 | 105,711,448 | ||
| nssv17377818 | Remapped | Perfect | NC_000014.8:g.1061 12789_106177785del | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 106,112,789 | 106,177,785 |