nsv4684449
- Organism: Homo sapiens
- Study:nstd192 (Smajlagić et al. 2020)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,595,826
- Publication(s):Smajlagic et al. 2020
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: 7630 SVs from 115 studies. See in: genome view
Overlapping variant regions from other studies: 7630 SVs from 115 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4684449 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 196,023,870 | 197,619,695 |
| nsv4684449 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 195,750,741 | 197,346,566 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv16215387 | deletion | mb1:o58 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16215387 | Remapped | Perfect | NC_000003.12:g.(?_ 196023870)_(197619 695_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 196,023,870 | 197,619,695 |
| nssv16215387 | Submitted genomic | NC_000003.11:g.(?_ 195750741)_(197346 566_?)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 195,750,741 | 197,346,566 |