nsv4385741
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:122,170
- 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: 1527 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 1494 SVs from 97 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4385741 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 20,415,730 | 20,537,899 |
| nsv4385741 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000019.9 | Chr19 | 20,598,536 | 20,720,705 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15682720 | Remapped | Perfect | NC_000019.10:g.(?_ 20415730)_(2053789 9_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 20,415,730 | 20,537,899 |
| nssv15685519 | Remapped | Perfect | NC_000019.10:g.(?_ 20415730)_(2053789 9_?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 20,415,730 | 20,537,899 |
| nssv15682720 | Submitted genomic | NC_000019.9:g.(?_2 0598536)_(20720705 _?)del | GRCh37 (hg19) | NC_000019.9 | Chr19 | 20,598,536 | 20,720,705 | ||
| nssv15685519 | Submitted genomic | NC_000019.9:g.(?_2 0598536)_(20720705 _?)del | GRCh37 (hg19) | NC_000019.9 | Chr19 | 20,598,536 | 20,720,705 |