nsv821006
- 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:49,515
- 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: 1077 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 1077 SVs from 84 studies. See in: genome view
Overlapping variant regions from other studies: 669 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821006 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 1,570,997 | 1,620,511 |
| nsv821006 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 1,551,643 | 1,601,157 |
| nsv821006 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000020.9 | Chr20 | 1,499,643 | 1,549,157 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420082 | Remapped | Perfect | NC_000020.11:g.(?_ 1570997)_(1620511_ ?)del | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 1,570,997 | 1,620,511 |
| nssv1420082 | Remapped | Perfect | NC_000020.10:g.(?_ 1551643)_(1601157_ ?)del | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 1,551,643 | 1,601,157 |
| nssv1420082 | Submitted genomic | NC_000020.9:g.(?_1 499643)_(1549157_? )del | NCBI36 (hg18) | NC_000020.9 | Chr20 | 1,499,643 | 1,549,157 |