nsv3071825
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- 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: 132 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 147 SVs from 37 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3071825 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 150,718,959 | 150,718,959 |
| nsv3071825 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 150,691,435 | 150,691,435 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14039090 | insertion | JWB-4007399 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14039090 | Remapped | Perfect | NC_000001.11:g.150 718959_150718960in s335 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 150,718,959 | 150,718,959 |
| nssv14039090 | Submitted genomic | NC_000001.10:g.150 691435_150691436in s335 | GRCh37 (hg19) | NC_000001.10 | Chr1 | 150,691,435 | 150,691,435 |