nsv821285
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:334,034
- Publication(s):Ju 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: 2215 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 2080 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 791 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821285 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 54,926,794 | 55,260,827 |
| nsv821285 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 54,694,268 | 55,028,303 |
| nsv821285 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 54,450,844 | 54,784,879 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420948 | Remapped | Good | NC_000011.10:g.(?_ 54926794)_(5526082 7_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 54,926,794 | 55,260,827 |
| nssv1420948 | Remapped | Perfect | NC_000011.9:g.(?_5 4694268)_(55028303 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 54,694,268 | 55,028,303 |
| nssv1420948 | Submitted genomic | NC_000011.8:g.(?_5 4450844)_(54784879 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 54,450,844 | 54,784,879 |