nsv5590655
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:78
- Publication(s):Ebert et al. 2021
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: 91 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 91 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5590655 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 75,409,956 | 75,410,033 | ||
| nsv5590655 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 75,121,000 | 75,121,077 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17075890 | deletion | SAMN00801888 | Sequencing | Sequence alignment | 2,004 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17075890 | Submitted genomic | NC_000011.10:g.754 09956_75410033delC | GRCh38 (hg38) | NC_000011.10 | Chr11 | 75,409,956 | 75,410,033 | ||
| nssv17075890 | Remapped | Perfect | NC_000011.9:g.7512 1000_75121077delC | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 75,121,000 | 75,121,077 |