nsv826392
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:90,167
- Publication(s):Park 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: 377 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 377 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 84 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv826392 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 59,411,856 | 59,502,022 |
| nsv826392 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 59,805,637 | 59,895,803 |
| nsv826392 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 58,091,904 | 58,182,070 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1441426 | Remapped | Perfect | NC_000012.12:g.(?_ 59411856)_(5950202 2_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 59,411,856 | 59,502,022 |
| nssv1441426 | Remapped | Perfect | NC_000012.11:g.(?_ 59805637)_(5989580 3_?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 59,805,637 | 59,895,803 |
| nssv1441426 | Submitted genomic | NC_000012.10:g.(?_ 58091904)_(5818207 0_?)del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 58,091,904 | 58,182,070 |