nsv5296272
- 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: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: 250 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 231 SVs from 26 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5296272 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000017.11 | Chr17 | 36,432,101 | 36,432,700 | ||
| nsv5296272 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003315949.1 | Chr17|NW_0 03315949.1 | 316,853 | 317,452 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16828439 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv16828439 | Submitted genomic | GRCh38.p13 | NC_000017.11 | Chr17 | 36,432,101 | 36,432,700 | ||
| nssv16828439 | Remapped | Perfect | GRCh37.p13 | First Pass | NW_003315949.1 | Chr17|NW_0 03315949.1 | 316,853 | 317,452 |