nsv4679951
- 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:374,577
- 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: 1522 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 1522 SVs from 72 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4679951 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 32,520,643 | 32,895,219 |
| nsv4679951 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000019.9 | Chr19 | 33,011,549 | 33,386,125 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16210045 | duplication | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16210045 | Remapped | Perfect | NC_000019.10:g.(?_ 32520643)_(3289521 9_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 32,520,643 | 32,895,219 |
| nssv16210045 | Submitted genomic | NC_000019.9:g.(?_3 3011549)_(33386125 _?)dup | GRCh37.p13 | NC_000019.9 | Chr19 | 33,011,549 | 33,386,125 |
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) |
|---|---|
| nssv16210045 | <0.001 |