nsv4378175
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:81,519
- 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: 1782 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 1394 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4378175 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 106,694,427 | 106,775,945 |
| nsv4378175 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 107,150,444 | 107,184,184 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15620479 | Remapped | Pass | NC_000014.9:g.(?_1 06694427)_(1067759 45_?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 106,694,427 | 106,775,945 |
| nssv15622132 | Remapped | Pass | NC_000014.9:g.(?_1 06694427)_(1067759 45_?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 106,694,427 | 106,775,945 |
| nssv15620479 | Submitted genomic | NC_000014.8:g.(?_1 07150444)_(1071841 84_?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 107,150,444 | 107,184,184 | ||
| nssv15622132 | Submitted genomic | NC_000014.8:g.(?_1 07150444)_(1071841 84_?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 107,150,444 | 107,184,184 |