nsv4679763
- 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:340,116
- 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: 1308 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 1308 SVs from 76 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4679763 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 146,727,790 | 147,067,905 |
| nsv4679763 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000007.13 | Chr7 | 146,424,882 | 146,764,997 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16209096 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16209096 | Remapped | Perfect | NC_000007.14:g.(?_ 146727790)_(147067 905_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 146,727,790 | 147,067,905 |
| nssv16209096 | Submitted genomic | NC_000007.13:g.(?_ 146424882)_(146764 997_?)del | GRCh37.p13 | NC_000007.13 | Chr7 | 146,424,882 | 146,764,997 |
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) |
|---|---|
| nssv16209096 | <0.001 |