nsv4387200
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:392,559
- Publication(s):Zarrei et al. 2019
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: 1136 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 1136 SVs from 79 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4387200 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 31,679,306 | 32,071,864 |
| nsv4387200 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 31,700,854 | 32,093,410 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15679595 | copy number gain | 182123 | SNP array | Genotyping | 24 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15679595 | Remapped | Good | NC_000011.10:g.(?_ 31679306)_(3207186 4_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 31,679,306 | 32,071,864 |
| nssv15679595 | Submitted genomic | NC_000011.9:g.(?_3 1700854)_(32093410 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 31,700,854 | 32,093,410 |