nsv4371136
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,151,132
- 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: 2892 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 2897 SVs from 94 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4371136 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 167,522,644 | 168,673,775 |
| nsv4371136 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 167,491,881 | 168,643,013 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15640180 | copy number gain | 14-0119-003 | SNP array | Genotyping | 15 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15640180 | Remapped | Perfect | NC_000001.11:g.(?_ 167522644)_(168673 775_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 167,522,644 | 168,673,775 |
| nssv15640180 | Submitted genomic | NC_000001.10:g.(?_ 167491881)_(168643 013_?)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 167,491,881 | 168,643,013 |