nsv433456
- 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:41,994
- 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: 662 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 662 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 29 SVs from 10 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433456 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 52,828,786 | 52,870,779 |
| nsv433456 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 53,332,039 | 53,374,032 |
| nsv433456 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000019.8 | Chr19 | 58,023,851 | 58,065,844 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463337 | Remapped | Perfect | NC_000019.10:g.(?_ 52828786)_(5287077 9_?)dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,828,786 | 52,870,779 |
| nssv463337 | Remapped | Perfect | NC_000019.9:g.(?_5 3332039)_(53374032 _?)dup | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,332,039 | 53,374,032 |
| nssv463337 | Submitted genomic | NC_000019.8:g.(?_5 8023851)_(58065844 _?)dup | NCBI35 (hg17) | NC_000019.8 | Chr19 | 58,023,851 | 58,065,844 |