nsv826349
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:32,650
- Publication(s):Park et al. 2010
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: 160 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 160 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 41 SVs from 12 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv826349 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 41,485,044 | 41,517,693 |
| nsv826349 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 41,878,846 | 41,911,495 |
| nsv826349 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 40,165,113 | 40,197,762 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1439200 | Remapped | Perfect | NC_000012.12:g.(?_ 41485044)_(4151769 3_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 41,485,044 | 41,517,693 |
| nssv1439200 | Remapped | Perfect | NC_000012.11:g.(?_ 41878846)_(4191149 5_?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 41,878,846 | 41,911,495 |
| nssv1439200 | Submitted genomic | NC_000012.10:g.(?_ 40165113)_(4019776 2_?)del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 40,165,113 | 40,197,762 |