nsv4368311
- 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:1,010,830
- 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: 3576 SVs from 98 studies. See in: genome view
Overlapping variant regions from other studies: 3615 SVs from 98 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4368311 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 43,307,154 | 44,317,983 |
| nsv4368311 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 41,384,516 | 42,395,351 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15668374 | copy number gain | 7-0197-003 | SNP array | Genotyping | 22 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15668374 | Remapped | Good | NC_000017.11:g.(?_ 43307154)_(4431798 3_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 43,307,154 | 44,317,983 |
| nssv15668374 | Submitted genomic | NC_000017.10:g.(?_ 41384516)_(4239535 1_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 41,384,516 | 42,395,351 |