nsv5210089
- 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:27,334
- 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: 167 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 168 SVs from 27 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5210089 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000002.12 | Chr2 | 233,247,201 | 233,274,534 | ||
| nsv5210089 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 234,155,847 | 234,183,180 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16793292 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv16793292 | Submitted genomic | GRCh38.p13 | NC_000002.12 | Chr2 | 233,247,201 | 233,274,534 | ||
| nssv16793292 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 234,155,847 | 234,183,180 |