nsv4745928
- Organism: Homo sapiens
- Study:nstd199 (Quan et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:153,661
- Publication(s):Quan 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: 998 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 251 SVs from 43 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4745928 | Remapped | Pass | GRCh38.p12 | Primary Assembly | Second Pass | NC_000008.11 | Chr8 | 141,735,285 | 141,888,945 |
| nsv4745928 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 142,754,604 | 142,825,878 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16264819 | deletion | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16264819 | Remapped | Pass | NC_000008.11:g.141 735285_141888945de l | GRCh38.p12 | Second Pass | NC_000008.11 | Chr8 | 141,735,285 | 141,888,945 |
| nssv16264819 | Submitted genomic | NC_000008.10:g.142 754604_142825878de l | GRCh37 (hg19) | NC_000008.10 | Chr8 | 142,754,604 | 142,825,878 |