nsv824701
- 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:141,766
- 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: 602 SVs from 66 studies. See in: genome view
Overlapping variant regions from other studies: 602 SVs from 66 studies. See in: genome view
Overlapping variant regions from other studies: 168 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv824701 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 106,366,070 | 106,507,835 |
| nsv824701 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 107,378,298 | 107,520,063 |
| nsv824701 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 107,447,474 | 107,589,239 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1441197 | Remapped | Perfect | NC_000008.11:g.(?_ 106366070)_(106507 835_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 106,366,070 | 106,507,835 |
| nssv1441197 | Remapped | Perfect | NC_000008.10:g.(?_ 107378298)_(107520 063_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 107,378,298 | 107,520,063 |
| nssv1441197 | Submitted genomic | NC_000008.9:g.(?_1 07447474)_(1075892 39_?)del | NCBI36 (hg18) | NC_000008.9 | Chr8 | 107,447,474 | 107,589,239 |