nsv3118368
- Organism: Homo sapiens
- Study:nstd149 (Gambin et al. 2017)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:387,919
- Publication(s):Gambin 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: 1965 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1965 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 | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3118368 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 3,028,131 | 3,416,049 |
| nsv3118368 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 2,885,653 | 3,273,571 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14109476 | copy number loss | CSMD1_Pt7 | Oligo aCGH | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14109476 | Remapped | Perfect | NC_000008.11:g.302 8131_3416049del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 3,028,131 | 3,416,049 |
| nssv14109476 | Submitted genomic | NC_000008.10:g.288 5653_3273571del | GRCh37 (hg19) | NC_000008.10 | Chr8 | 2,885,653 | 3,273,571 |