nsv6627193
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,968,074
- Publication(s):Zarrei et al. 2023
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: 9370 SVs from 127 studies. See in: genome view
Overlapping variant regions from other studies: 10226 SVs from 131 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6627193 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 22,646,834 | 24,614,907 |
| nsv6627193 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 22,989,304 | 25,010,874 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18284487 | duplication | OSC0269 | SNP array | Probe signal intensity | 7 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18284487 | Remapped | Good | NC_000022.11:g.(?_ 22646834)_(2461490 7_?)dup | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 22,646,834 | 24,614,907 |
| nssv18284487 | Submitted genomic | NC_000022.10:g.(?_ 22989304)_(2501087 4_?)dup | GRCh37 (hg19) | NC_000022.10 | Chr22 | 22,989,304 | 25,010,874 |