nsv4680391
- Organism: Homo sapiens
- Study:nstd189 (Perez-Palma 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:326,819
- Publication(s):Pérez-Palma 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: 1621 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 1621 SVs from 89 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4680391 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 83,825,227 | 84,152,045 |
| nsv4680391 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000016.9 | Chr16 | 83,858,832 | 84,185,650 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16210513 | deletion | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16210513 | Remapped | Perfect | NC_000016.10:g.(?_ 83825227)_(8415204 5_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 83,825,227 | 84,152,045 |
| nssv16210513 | Submitted genomic | NC_000016.9:g.(?_8 3858832)_(84185650 _?)del | GRCh37.p13 | NC_000016.9 | Chr16 | 83,858,832 | 84,185,650 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) |
|---|---|
| nssv16210513 | <0.001 |