nsv821341
- 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:60,602
- 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: 429 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 427 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 117 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821341 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 47,533,665 | 47,594,266 |
| nsv821341 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 45,611,031 | 45,671,632 |
| nsv821341 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 42,966,030 | 43,026,631 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1419946 | Remapped | Perfect | NC_000017.11:g.(?_ 47533665)_(4759426 6_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 47,533,665 | 47,594,266 |
| nssv1419946 | Remapped | Perfect | NC_000017.10:g.(?_ 45611031)_(4567163 2_?)dup | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 45,611,031 | 45,671,632 |
| nssv1419946 | Submitted genomic | NC_000017.9:g.(?_4 2966030)_(43026631 _?)dup | NCBI36 (hg18) | NC_000017.9 | Chr17 | 42,966,030 | 43,026,631 |