nsv3114421
- 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:2,123
- 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: 151 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 151 SVs from 36 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3114421 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 12,562,685 | 12,564,807 |
| nsv3114421 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 12,656,542 | 12,658,664 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14099219 | Remapped | Perfect | NC_000016.10:g.(?_ 12562685)_(1256480 7_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 12,562,685 | 12,564,807 |
| nssv14099222 | Remapped | Perfect | NC_000016.10:g.(?_ 12562685)_(1256480 7_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 12,562,685 | 12,564,807 |
| nssv14099219 | Submitted genomic | NC_000016.9:g.(?_1 2656542)_(12658664 _?)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 12,656,542 | 12,658,664 | ||
| nssv14099222 | Submitted genomic | NC_000016.9:g.(?_1 2656542)_(12658664 _?)del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 12,656,542 | 12,658,664 |