nsv821598
- 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:120,704
- 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: 1585 SVs from 76 studies. See in: genome view
Overlapping variant regions from other studies: 1548 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 741 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821598 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 10,627,450 | 10,748,153 |
| nsv821598 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000021.8 | Chr21 | 10,764,304 | 10,885,007 |
| nsv821598 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000021.7 | Chr21 | 9,786,175 | 9,906,878 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420118 | Remapped | Perfect | NC_000021.9:g.(?_1 0627450)_(10748153 _?)dup | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 10,627,450 | 10,748,153 |
| nssv1420118 | Remapped | Perfect | NC_000021.8:g.(?_1 0764304)_(10885007 _?)dup | GRCh37.p13 | First Pass | NC_000021.8 | Chr21 | 10,764,304 | 10,885,007 |
| nssv1420118 | Submitted genomic | NC_000021.7:g.(?_9 786175)_(9906878_? )dup | NCBI36 (hg18) | NC_000021.7 | Chr21 | 9,786,175 | 9,906,878 |