nsv4684427
- 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:1,575,002
- 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: 6006 SVs from 127 studies. See in: genome view
Overlapping variant regions from other studies: 6006 SVs from 127 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4684427 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 30,647,899 | 32,222,900 |
| nsv4684427 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 30,940,102 | 32,515,101 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv16215367 | duplication | mb2:o20 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16215367 | Remapped | Perfect | NC_000015.10:g.(?_ 30647899)_(3222290 0_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 30,647,899 | 32,222,900 |
| nssv16215367 | Submitted genomic | NC_000015.9:g.(?_3 0940102)_(32515101 _?)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 30,940,102 | 32,515,101 |