nsv828047
- 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:105,174
- 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: 374 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 374 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 100 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv828047 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 53,035,785 | 53,140,958 |
| nsv828047 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 51,113,145 | 51,218,319 |
| nsv828047 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 48,468,144 | 48,573,318 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1421564 | Remapped | Good | NC_000017.11:g.(?_ 53035785)_(5314095 8_?)del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 53,035,785 | 53,140,958 |
| nssv1421564 | Remapped | Perfect | NC_000017.10:g.(?_ 51113145)_(5121831 9_?)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 51,113,145 | 51,218,319 |
| nssv1421564 | Submitted genomic | NC_000017.9:g.(?_4 8468144)_(48573318 _?)del | NCBI36 (hg18) | NC_000017.9 | Chr17 | 48,468,144 | 48,573,318 |