nsv820422
- 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:23,732
- 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: 494 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 494 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 201 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820422 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 54,686,132 | 54,709,863 |
| nsv820422 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 56,445,892 | 56,469,623 |
| nsv820422 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 56,115,898 | 56,139,629 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420876 | Remapped | Perfect | NC_000010.11:g.(?_ 54686132)_(5470986 3_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 54,686,132 | 54,709,863 |
| nssv1420876 | Remapped | Perfect | NC_000010.10:g.(?_ 56445892)_(5646962 3_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 56,445,892 | 56,469,623 |
| nssv1420876 | Submitted genomic | NC_000010.9:g.(?_5 6115898)_(56139629 _?)dup | NCBI36 (hg18) | NC_000010.9 | Chr10 | 56,115,898 | 56,139,629 |