nsv433412
- 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:43,662
- 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: 148 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 9 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433412 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 59,098,182 | 59,141,843 |
| nsv433412 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 60,857,942 | 60,901,603 |
| nsv433412 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 60,527,948 | 60,571,609 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463293 | Remapped | Perfect | NC_000010.11:g.(?_ 59098182)_(5914184 3_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 59,098,182 | 59,141,843 |
| nssv463293 | Remapped | Perfect | NC_000010.10:g.(?_ 60857942)_(6090160 3_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 60,857,942 | 60,901,603 |
| nssv463293 | Submitted genomic | NC_000010.8:g.(?_6 0527948)_(60571609 _?)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 60,527,948 | 60,571,609 |