nsv3118312
- 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:4,972
- 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: 320 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 320 SVs from 59 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3118312 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 49,306,969 | 49,311,940 |
| nsv3118312 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 49,534,108 | 49,539,079 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14102526 | Remapped | Perfect | NC_000002.12:g.(?_ 49306969)_(4931194 0_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 49,306,969 | 49,311,940 |
| nssv14106206 | Remapped | Perfect | NC_000002.12:g.(?_ 49306969)_(4931194 0_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 49,306,969 | 49,311,940 |
| nssv14102526 | Submitted genomic | NC_000002.11:g.(?_ 49534108)_(4953907 9_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 49,534,108 | 49,539,079 | ||
| nssv14106206 | Submitted genomic | NC_000002.11:g.(?_ 49534108)_(4953907 9_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 49,534,108 | 49,539,079 |