nsv820605
- 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:41,905
- 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: 417 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 417 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 162 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820605 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 131,723,141 | 131,765,045 |
| nsv820605 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 132,644,296 | 132,686,200 |
| nsv820605 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 132,863,746 | 132,905,650 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420443 | Remapped | Perfect | NC_000004.12:g.(?_ 131723141)_(131765 045_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 131,723,141 | 131,765,045 |
| nssv1420443 | Remapped | Perfect | NC_000004.11:g.(?_ 132644296)_(132686 200_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 132,644,296 | 132,686,200 |
| nssv1420443 | Submitted genomic | NC_000004.10:g.(?_ 132863746)_(132905 650_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 132,863,746 | 132,905,650 |