nsv5946832
- 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:87,150
- 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: 2083 SVs from 98 studies. See in: genome view
Overlapping variant regions from other studies: 1821 SVs from 96 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5946832 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000014.9 | Chr14 | 105,773,750 | 105,860,899 | ||
| nsv5946832 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 106,240,087 | 106,320,043 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17382507 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17382507 | Submitted genomic | NC_000014.9:g.1057 73750_105860899del | GRCh38 (hg38) | NC_000014.9 | Chr14 | 105,773,750 | 105,860,899 | ||
| nssv17382507 | Remapped | Pass | NC_000014.8:g.1062 40087_106320043del | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 106,240,087 | 106,320,043 |