nsv4376851
- 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:823,502
- 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: 2611 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 2611 SVs from 81 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4376851 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 76,576,122 | 77,399,623 |
| nsv4376851 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 77,042,465 | 77,865,966 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15612610 | copy number gain | 1-0121-003 | SNP array | Genotyping | 31 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15612610 | Remapped | Perfect | NC_000014.9:g.(?_7 6576122)_(77399623 _?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 76,576,122 | 77,399,623 |
| nssv15612610 | Submitted genomic | NC_000014.8:g.(?_7 7042465)_(77865966 _?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 77,042,465 | 77,865,966 |