nsv4369340
- 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:55,721
- 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: 317 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 317 SVs from 59 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4369340 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 67,581,535 | 67,637,255 |
| nsv4369340 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 67,349,006 | 67,404,726 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15676376 | copy number gain | 209352 | SNP array | Genotyping | 33 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15676376 | Remapped | Perfect | NC_000011.10:g.(?_ 67581535)_(6763725 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 67,581,535 | 67,637,255 |
| nssv15676376 | Submitted genomic | NC_000011.9:g.(?_6 7349006)_(67404726 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 67,349,006 | 67,404,726 |