nsv433457
- Organism: Homo sapiens
- Study:nstd14 (Cooper et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:64,206
- Publication(s):Cooper et al. 2008
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: 535 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 535 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 13 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433457 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 39,528,421 | 39,592,626 |
| nsv433457 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 40,900,348 | 40,964,553 |
| nsv433457 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000021.7 | Chr21 | 39,822,218 | 39,886,423 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463338 | Remapped | Perfect | NC_000021.9:g.(?_3 9528421)_(39592626 _?)dup | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 39,528,421 | 39,592,626 |
| nssv463338 | Remapped | Perfect | NC_000021.8:g.(?_4 0900348)_(40964553 _?)dup | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 40,900,348 | 40,964,553 |
| nssv463338 | Submitted genomic | NC_000021.7:g.(?_3 9822218)_(39886423 _?)dup | NCBI35 (hg17) | NC_000021.7 | Chr21 | 39,822,218 | 39,886,423 |