nsv4373006
- 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:85,352
- 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: 422 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 423 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4373006 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 18,776,747 | 18,862,098 |
| nsv4373006 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000024.9 | ChrY | 20,938,633 | 21,023,984 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15647880 | copy number gain | 2-1303-003 | SNP array | Genotyping | 22 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15647880 | Remapped | Perfect | NC_000024.10:g.(?_ 18776747)_(1886209 8_?)dup | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 18,776,747 | 18,862,098 |
| nssv15647880 | Submitted genomic | NC_000024.9:g.(?_2 0938633)_(21023984 _?)dup | GRCh37 (hg19) | NC_000024.9 | ChrY | 20,938,633 | 21,023,984 |