nsv5946041
- 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:113,863
- 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: 2919 SVs from 102 studies. See in: genome view
Overlapping variant regions from other studies: 2754 SVs from 100 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5946041 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000014.9 | Chr14 | 105,745,229 | 105,859,091 | ||
| nsv5946041 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 106,211,566 | 106,320,043 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17373966 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17373966 | Submitted genomic | NC_000014.9:g.1057 45229_105859091del | GRCh38 (hg38) | NC_000014.9 | Chr14 | 105,745,229 | 105,859,091 | ||
| nssv17373966 | Remapped | Good | NC_000014.8:g.1062 11566_106320043del | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 106,211,566 | 106,320,043 |