nsv6632491
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:149,046
- 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: 421 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 421 SVs from 43 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6632491 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 134,610,608 | 134,759,653 |
| nsv6632491 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 135,622,851 | 135,771,896 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18297262 | duplication | OSC4864 | SNP array | Probe signal intensity | nssv18297261, nssv18296935, nssv18296936 |
| nssv18297535 | duplication | OSC4823 | SNP array | Probe signal intensity | 10 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18297262 | Remapped | Perfect | NC_000008.11:g.(?_ 134610608)_(134759 653_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 134,610,608 | 134,759,653 |
| nssv18297535 | Remapped | Perfect | NC_000008.11:g.(?_ 134610608)_(134759 653_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 134,610,608 | 134,759,653 |
| nssv18297262 | Submitted genomic | NC_000008.10:g.(?_ 135622851)_(135771 896_?)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 135,622,851 | 135,771,896 | ||
| nssv18297535 | Submitted genomic | NC_000008.10:g.(?_ 135622851)_(135771 896_?)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 135,622,851 | 135,771,896 |