nsv4381298
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:83,420
- Publication(s):Zarrei et al. 2019
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: 394 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 405 SVs from 63 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4381298 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 55,309,180 | 55,392,599 |
| nsv4381298 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 55,076,656 | 55,160,075 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15628724 | Remapped | Perfect | NC_000011.10:g.(?_ 55309180)_(5539259 9_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 55,309,180 | 55,392,599 |
| nssv15628816 | Remapped | Perfect | NC_000011.10:g.(?_ 55309180)_(5539259 9_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 55,309,180 | 55,392,599 |
| nssv15628724 | Submitted genomic | NC_000011.9:g.(?_5 5076656)_(55160075 _?)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 55,076,656 | 55,160,075 | ||
| nssv15628816 | Submitted genomic | NC_000011.9:g.(?_5 5076656)_(55160075 _?)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 55,076,656 | 55,160,075 |