nsv4373698
- 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:253,132
- 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: 859 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 858 SVs from 73 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4373698 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 69,891,295 | 70,144,426 |
| nsv4373698 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 70,118,427 | 70,371,558 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15685310 | copy number loss | OCD117-B_1699 | SNP array | Genotyping | 29 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15685310 | Remapped | Perfect | NC_000002.12:g.(?_ 69891295)_(7014442 6_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 69,891,295 | 70,144,426 |
| nssv15685310 | Submitted genomic | NC_000002.11:g.(?_ 70118427)_(7037155 8_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 70,118,427 | 70,371,558 |