nsv4680228
- 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:248,758
- 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: 1379 SVs from 103 studies. See in: genome view
Overlapping variant regions from other studies: 1379 SVs from 103 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4680228 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 4,946,035 | 5,194,792 |
| nsv4680228 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000011.9 | Chr11 | 4,967,265 | 5,216,022 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16210941 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16210941 | Remapped | Perfect | NC_000011.10:g.(?_ 4946035)_(5194792_ ?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 4,946,035 | 5,194,792 |
| nssv16210941 | Submitted genomic | NC_000011.9:g.(?_4 967265)_(5216022_? )del | GRCh37.p13 | NC_000011.9 | Chr11 | 4,967,265 | 5,216,022 |
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) |
|---|---|
| nssv16210941 | <0.001 |