nsv433225
- 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:100,806
- 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: 519 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 519 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433225 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 13,040,645 | 13,141,450 |
| nsv433225 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 13,040,757 | 13,141,562 |
| nsv433225 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000005.8 | Chr5 | 13,093,757 | 13,194,562 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463106 | Remapped | Perfect | NC_000005.10:g.(?_ 13040645)_(1314145 0_?)del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 13,040,645 | 13,141,450 |
| nssv463106 | Remapped | Perfect | NC_000005.9:g.(?_1 3040757)_(13141562 _?)del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 13,040,757 | 13,141,562 |
| nssv463106 | Submitted genomic | NC_000005.8:g.(?_1 3093757)_(13194562 _?)del | NCBI35 (hg17) | NC_000005.8 | Chr5 | 13,093,757 | 13,194,562 |