nsv4369695
- 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:67,260
- 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: 1688 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 1596 SVs from 95 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4369695 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 18,950,000 | 19,017,259 |
| nsv4369695 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 18,937,513 | 19,004,772 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15644639 | Remapped | Perfect | NC_000022.11:g.(?_ 18950000)_(1901725 9_?)dup | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 18,950,000 | 19,017,259 |
| nssv15663458 | Remapped | Perfect | NC_000022.11:g.(?_ 18950000)_(1901725 9_?)dup | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 18,950,000 | 19,017,259 |
| nssv15644639 | Submitted genomic | NC_000022.10:g.(?_ 18937513)_(1900477 2_?)dup | GRCh37 (hg19) | NC_000022.10 | Chr22 | 18,937,513 | 19,004,772 | ||
| nssv15663458 | Submitted genomic | NC_000022.10:g.(?_ 18937513)_(1900477 2_?)dup | GRCh37 (hg19) | NC_000022.10 | Chr22 | 18,937,513 | 19,004,772 |