nsv820565
- 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:13,603
- 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: 946 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 946 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 561 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820565 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 78,337,626 | 78,351,228 |
| nsv820565 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 78,371,523 | 78,385,125 |
| nsv820565 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 76,929,024 | 76,942,626 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1419892 | Remapped | Perfect | NC_000016.10:g.(?_ 78337626)_(7835122 8_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 78,337,626 | 78,351,228 |
| nssv1419892 | Remapped | Perfect | NC_000016.9:g.(?_7 8371523)_(78385125 _?)del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 78,371,523 | 78,385,125 |
| nssv1419892 | Submitted genomic | NC_000016.8:g.(?_7 6929024)_(76942626 _?)del | NCBI36 (hg18) | NC_000016.8 | Chr16 | 76,929,024 | 76,942,626 |