nsv821177
- 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:32,437
- 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: 339 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 338 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 116 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821177 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 57,822,251 | 57,854,687 |
| nsv821177 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 57,881,957 | 57,914,393 |
| nsv821177 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 57,885,899 | 57,918,335 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420657 | Remapped | Perfect | NC_000007.14:g.(?_ 57822251)_(5785468 7_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 57,822,251 | 57,854,687 |
| nssv1420657 | Remapped | Perfect | NC_000007.13:g.(?_ 57881957)_(5791439 3_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 57,881,957 | 57,914,393 |
| nssv1420657 | Submitted genomic | NC_000007.12:g.(?_ 57885899)_(5791833 5_?)dup | NCBI36 (hg18) | NC_000007.12 | Chr7 | 57,885,899 | 57,918,335 |