nsv818102
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:129,312
- Publication(s):Wang et al. 2007
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: 584 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 584 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 17 SVs from 7 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv818102 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 184,345,883 | 184,475,194 |
| nsv818102 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 185,210,610 | 185,339,921 |
| nsv818102 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000002.9 | Chr2 | 185,036,116 | 185,165,427 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1416921 | Remapped | Perfect | NC_000002.12:g.(?_ 184345883)_(184475 194_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 184,345,883 | 184,475,194 |
| nssv1416921 | Remapped | Perfect | NC_000002.11:g.(?_ 185210610)_(185339 921_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 185,210,610 | 185,339,921 |
| nssv1416921 | Submitted genomic | NC_000002.9:g.(?_1 85036116)_(1851654 27_?)del | NCBI35 (hg17) | NC_000002.9 | Chr2 | 185,036,116 | 185,165,427 |