nsv4433422
- Organism: Homo sapiens
- Study:nstd172 (Deng et al. 2019)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,005
- Publication(s):Deng 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: 173 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 173 SVs from 56 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4433422 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 35,249,238 | 35,250,242 |
| nsv4433422 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000022.10 | Chr22 | 35,645,231 | 35,646,235 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15748631 | deletion | MDQ045 | Sequencing | Sequence alignment | 724 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15748631 | Remapped | Perfect | NC_000022.11:g.352 49238_35250242del | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 35,249,238 | 35,250,242 |
| nssv15748631 | Submitted genomic | NC_000022.10:g.356 45231_35646235del | GRCh37.p13 | NC_000022.10 | Chr22 | 35,645,231 | 35,646,235 |