nsv3069207
- 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:864
- 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: 289 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 289 SVs from 65 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3069207 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 108,238,962 | 108,239,825 |
| nsv3069207 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 108,855,418 | 108,856,281 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14041409 | deletion | JWB-4073549 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14041409 | Remapped | Perfect | NC_000002.12:g.108 238962_108239825de l864 | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 108,238,962 | 108,239,825 |
| nssv14041409 | Submitted genomic | NC_000002.11:g.108 855418_108856281de l864 | GRCh37 (hg19) | NC_000002.11 | Chr2 | 108,855,418 | 108,856,281 |