nsv4370736
- 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:289,977
- 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: 1632 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 1501 SVs from 93 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4370736 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 35,215,224 | 35,505,200 |
| nsv4370736 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 34,449,595 | 34,739,571 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15660795 | Remapped | Perfect | NC_000016.10:g.(?_ 35215224)_(3550520 0_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,215,224 | 35,505,200 |
| nssv15678759 | Remapped | Perfect | NC_000016.10:g.(?_ 35215224)_(3550520 0_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 35,215,224 | 35,505,200 |
| nssv15660795 | Submitted genomic | NC_000016.9:g.(?_3 4449595)_(34739571 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,449,595 | 34,739,571 | ||
| nssv15678759 | Submitted genomic | NC_000016.9:g.(?_3 4449595)_(34739571 _?)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 34,449,595 | 34,739,571 |