nsv819828
- Organism: Homo sapiens
- Study:nstd43 (Kim et al. 2009)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:48,734
- Publication(s):Kim et al. 2009
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: 621 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 621 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 283 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819828 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 21,525,686 | 21,574,419 |
| nsv819828 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 21,537,007 | 21,585,740 |
| nsv819828 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 21,444,508 | 21,493,241 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418744 | copy number gain | SAMN00002681 | Oligo aCGH | Probe signal intensity | 1,333 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418744 | Remapped | Perfect | NC_000016.10:g.(?_ 21525686)_(2157441 9_?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 21,525,686 | 21,574,419 |
| nssv1418744 | Remapped | Perfect | NC_000016.9:g.(?_2 1537007)_(21585740 _?)dup | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 21,537,007 | 21,585,740 |
| nssv1418744 | Submitted genomic | NC_000016.8:g.(?_2 1444508)_(21493241 _?)dup | NCBI36 (hg18) | NC_000016.8 | Chr16 | 21,444,508 | 21,493,241 |