nsv3070777
- 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:1,183
- 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: 482 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 482 SVs from 57 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3070777 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 716,038 | 717,220 |
| nsv3070777 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 709,827 | 711,009 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14039016 | deletion | 1104685132287 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14039016 | Remapped | Perfect | NC_000004.12:g.716 038_717220del1183 | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 716,038 | 717,220 |
| nssv14039016 | Submitted genomic | NC_000004.11:g.709 827_711009del1183 | GRCh37 (hg19) | NC_000004.11 | Chr4 | 709,827 | 711,009 |