nsv3070105
- 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:890
- Data Source:BCMHGSC_JDW
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: 257 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 255 SVs from 61 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3070105 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 62,672,898 | 62,673,787 |
| nsv3070105 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000020.10 | Chr20 | 61,304,250 | 61,305,139 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14039026 | deletion | JWB-4084452 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14039026 | Remapped | Perfect | NC_000020.11:g.626 72898_62673787del8 90 | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 62,672,898 | 62,673,787 |
| nssv14039026 | Submitted genomic | NC_000020.10:g.613 04250_61305139del8 90 | GRCh37 (hg19) | NC_000020.10 | Chr20 | 61,304,250 | 61,305,139 |