nsv3067420
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,034
- Data Source:HUMANGENOME_JCVI
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: 198 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 203 SVs from 39 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3067420 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 226,956,026 | 226,957,059 |
| nsv3067420 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 227,143,727 | 227,144,760 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14042747 | deletion | 1104685057300 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14042747 | Remapped | Perfect | NC_000001.11:g.226 956026_226957059de l1034 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 226,956,026 | 226,957,059 |
| nssv14042747 | Submitted genomic | NC_000001.10:g.227 143727_227144760de l1034 | GRCh37 (hg19) | NC_000001.10 | Chr1 | 227,143,727 | 227,144,760 |