nsv1067818
- Organism: Homo sapiens
- Study:nstd98 (Campbell et al. 2014b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,375,992
- Publication(s):Campbell et al. 2014
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: 7653 SVs from 113 studies. See in: genome view
Overlapping variant regions from other studies: 7653 SVs from 113 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv1067818 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 112,419,960 | 112,420,012 | 115,795,899 | 115,795,951 |
| nsv1067818 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 112,138,807 | 112,138,859 | 115,514,746 | 115,514,798 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3761530 | deletion | Sequencing | Sequence alignment |
| nssv3761537 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3761530 | Remapped | Perfect | NC_000003.12:g.(11 2419960_112420012) _(115795899_115795 951)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 112,419,960 | 112,420,012 | 115,795,899 | 115,795,951 |
| nssv3761537 | Remapped | Perfect | NC_000003.12:g.(11 2419960_112420012) _(115795899_115795 951)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 112,419,960 | 112,420,012 | 115,795,899 | 115,795,951 |
| nssv3761530 | Submitted genomic | NC_000003.11:g.(11 2138807_112138859) _(115514746_115514 798)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 112,138,807 | 112,138,859 | 115,514,746 | 115,514,798 | ||
| nssv3761537 | Submitted genomic | NC_000003.11:g.(11 2138807_112138859) _(115514746_115514 798)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 112,138,807 | 112,138,859 | 115,514,746 | 115,514,798 |