nsv821123
- 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:62,888
- 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: 315 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 315 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821123 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 131,660,253 | 131,723,140 |
| nsv821123 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 132,581,408 | 132,644,295 |
| nsv821123 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 132,800,858 | 132,863,745 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420442 | Remapped | Perfect | NC_000004.12:g.(?_ 131660253)_(131723 140_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 131,660,253 | 131,723,140 |
| nssv1420442 | Remapped | Perfect | NC_000004.11:g.(?_ 132581408)_(132644 295_?)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 132,581,408 | 132,644,295 |
| nssv1420442 | Submitted genomic | NC_000004.10:g.(?_ 132800858)_(132863 745_?)dup | NCBI36 (hg18) | NC_000004.10 | Chr4 | 132,800,858 | 132,863,745 |