nsv3117989
- Organism: Homo sapiens
- Study:nstd145 (Lu et al. 2017)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:10,116
- Publication(s):Lu et al. 2017
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: 437 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 437 SVs from 83 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3117989 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 193,157,765 | 193,167,880 |
| nsv3117989 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 192,875,554 | 192,885,669 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14105605 | Remapped | Perfect | NC_000003.12:g.(?_ 193157765)_(193167 880_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 193,157,765 | 193,167,880 |
| nssv14108188 | Remapped | Perfect | NC_000003.12:g.(?_ 193157765)_(193167 880_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 193,157,765 | 193,167,880 |
| nssv14105605 | Submitted genomic | NC_000003.11:g.(?_ 192875554)_(192885 669_?)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 192,875,554 | 192,885,669 | ||
| nssv14108188 | Submitted genomic | NC_000003.11:g.(?_ 192875554)_(192885 669_?)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 192,875,554 | 192,885,669 |