nsv433218
- 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:91,420
- 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: 414 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 414 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 56 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433218 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 28,639,440 | 28,730,859 |
| nsv433218 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 28,641,062 | 28,732,481 |
| nsv433218 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000004.9 | Chr4 | 28,317,331 | 28,408,750 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463099 | Remapped | Perfect | NC_000004.12:g.(?_ 28639440)_(2873085 9_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 28,639,440 | 28,730,859 |
| nssv463099 | Remapped | Perfect | NC_000004.11:g.(?_ 28641062)_(2873248 1_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 28,641,062 | 28,732,481 |
| nssv463099 | Submitted genomic | NC_000004.9:g.(?_2 8317331)_(28408750 _?)del | NCBI35 (hg17) | NC_000004.9 | Chr4 | 28,317,331 | 28,408,750 |