nsv3068717
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:delins
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,371
- 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: 326 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 326 SVs from 53 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3068717 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 1,429,813 | 1,431,183 |
| nsv3068717 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 1,451,043 | 1,452,413 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14040383 | delins | 1104685068926 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14040383 | Remapped | Perfect | NC_000011.10:g.142 9813_1431183delins 2881 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 1,429,813 | 1,431,183 |
| nssv14040383 | Submitted genomic | NC_000011.9:g.1451 043_1452413delins2 881 | GRCh37 (hg19) | NC_000011.9 | Chr11 | 1,451,043 | 1,452,413 |