nsv5670120
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:125
- Publication(s):Ebert et al. 2021
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|
| nsv5670120 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | KI270740.1 | ChrY|KI270 740.1 | 29,890 | 30,014 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17171352 | deletion | SAMN00006579 | Sequencing | Sequence alignment | 23,265 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Assembly | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|
| nssv17171352 | Submitted genomic | GRCh38 (hg38) | KI270740.1 | ChrY|KI270 740.1 | 29,890 | 30,014 |