nsv4382895
- 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:173,329
- 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: 2072 SVs from 96 studies. See in: genome view
Overlapping variant regions from other studies: 2072 SVs from 96 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4382895 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 68,501,374 | 68,674,702 |
| nsv4382895 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 69,367,092 | 69,540,420 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15674692 | copy number gain | 185283 | SNP array | Genotyping | 16 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15674692 | Remapped | Perfect | NC_000004.12:g.(?_ 68501374)_(6867470 2_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 68,501,374 | 68,674,702 |
| nssv15674692 | Submitted genomic | NC_000004.11:g.(?_ 69367092)_(6954042 0_?)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 69,367,092 | 69,540,420 |