nsv820432
- 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:12,727
- 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: 318 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 318 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 151 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820432 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 28,696,869 | 28,709,595 |
| nsv820432 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 28,708,190 | 28,720,916 |
| nsv820432 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 28,615,691 | 28,628,417 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1421174 | Remapped | Perfect | NC_000016.10:g.(?_ 28696869)_(2870959 5_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 28,696,869 | 28,709,595 |
| nssv1421174 | Remapped | Perfect | NC_000016.9:g.(?_2 8708190)_(28720916 _?)del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 28,708,190 | 28,720,916 |
| nssv1421174 | Submitted genomic | NC_000016.8:g.(?_2 8615691)_(28628417 _?)del | NCBI36 (hg18) | NC_000016.8 | Chr16 | 28,615,691 | 28,628,417 |