nsv959592
- Organism: Homo sapiens
- Study:nstd86 (Poultney et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:61,569
- Publication(s):Poultney et al. 2013
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: 634 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 634 SVs from 68 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959592 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 101,382,092 | 101,443,660 |
| nsv959592 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 101,922,297 | 101,983,865 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3020666 | duplication | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3020666 | Remapped | Good | NC_000015.10:g.(10 1366332_101366332) _(101642477_101642 477)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 101,366,332 | 101,366,332 | 101,642,477 | 101,642,477 |
| nssv3020666 | Submitted genomic | NC_000015.9:g.(101 906537_101922297)_ (101983865_1021826 80)dup | GRCh37 (hg19) | NC_000015.9 | Chr15 | 101,906,537 | 101,922,297 | 101,983,865 | 102,182,680 |