nsv821496
- 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:18,546
- 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: 463 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 463 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 157 SVs from 22 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821496 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 122,598,831 | 122,617,376 |
| nsv821496 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 124,358,347 | 124,376,892 |
| nsv821496 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 124,348,337 | 124,366,882 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420899 | Remapped | Perfect | NC_000010.11:g.(?_ 122598831)_(122617 376_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 122,598,831 | 122,617,376 |
| nssv1420899 | Remapped | Perfect | NC_000010.10:g.(?_ 124358347)_(124376 892_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 124,358,347 | 124,376,892 |
| nssv1420899 | Submitted genomic | NC_000010.9:g.(?_1 24348337)_(1243668 82_?)dup | NCBI36 (hg18) | NC_000010.9 | Chr10 | 124,348,337 | 124,366,882 |