nsv4386330
- 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:120,666
- 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: 1814 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1814 SVs from 93 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4386330 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 24,112,594 | 24,233,259 |
| nsv4386330 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 24,357,741 | 24,478,406 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15613814 | Remapped | Perfect | NC_000015.10:g.(?_ 24112594)_(2423325 9_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 24,112,594 | 24,233,259 |
| nssv15687137 | Remapped | Perfect | NC_000015.10:g.(?_ 24112594)_(2423325 9_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 24,112,594 | 24,233,259 |
| nssv15613814 | Submitted genomic | NC_000015.9:g.(?_2 4357741)_(24478406 _?)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 24,357,741 | 24,478,406 | ||
| nssv15687137 | Submitted genomic | NC_000015.9:g.(?_2 4357741)_(24478406 _?)del | GRCh37 (hg19) | NC_000015.9 | Chr15 | 24,357,741 | 24,478,406 |