nsv5217222
- Organism: Homo sapiens
- Study:nstd204 (Chen 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:1,051,600
- Publication(s):Chen et al. 2021
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: 3221 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 3229 SVs from 96 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5217222 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000003.12 | Chr3 | 60,347,401 | 61,399,000 | ||
| nsv5217222 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 60,333,132 | 61,384,674 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16853165 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv16853165 | Submitted genomic | GRCh38.p13 | NC_000003.12 | Chr3 | 60,347,401 | 61,399,000 | ||
| nssv16853165 | Remapped | Good | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 60,333,132 | 61,384,674 |