nsv3070942
- 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:2,776
- 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 45 studies. See in: genome view
Overlapping variant regions from other studies: 198 SVs from 45 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3070942 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 100,309,671 | 100,312,446 |
| nsv3070942 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 99,907,294 | 99,910,069 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14042767 | deletion | 1104685074419 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14042767 | Remapped | Perfect | NC_000007.14:g.100 309671_100312446de l2776 | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 100,309,671 | 100,312,446 |
| nssv14042767 | Submitted genomic | NC_000007.13:g.999 07294_99910069del2 776 | GRCh37 (hg19) | NC_000007.13 | Chr7 | 99,907,294 | 99,910,069 |