nsv2758533
- Organism: Homo sapiens
- Study:nstd130 (Leppa et al. 2016)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:96,470
- Publication(s):Leppa et al. 2016
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: 463 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 463 SVs from 58 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv2758533 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 49,598,641 | 49,695,110 |
| nsv2758533 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 50,065,359 | 50,161,828 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv13614578 | deletion | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv13614578 | Remapped | Perfect | NC_000014.9:g.(?_4 9598641)_(49695110 _?)del | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 49,598,641 | 49,695,110 |
| nssv13614578 | Submitted genomic | NC_000014.8:g.(?_5 0065359)_(50161828 _?)del | GRCh37 (hg19) | NC_000014.8 | Chr14 | 50,065,359 | 50,161,828 |