nsv4376448
- 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:482,056
- 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: 3422 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 4014 SVs from 95 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4376448 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 50,339,293 | 50,821,348 |
| nsv4376448 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 50,298,464 | 51,205,141 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15643391 | Remapped | Pass | NC_000011.10:g.(?_ 50339293)_(5082134 8_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,339,293 | 50,821,348 |
| nssv15644177 | Remapped | Pass | NC_000011.10:g.(?_ 50339293)_(5082134 8_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,339,293 | 50,821,348 |
| nssv15643391 | Submitted genomic | NC_000011.9:g.(?_5 0298464)_(51205141 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,298,464 | 51,205,141 | ||
| nssv15644177 | Submitted genomic | NC_000011.9:g.(?_5 0298464)_(51205141 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,298,464 | 51,205,141 |