nsv3070456
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:mobile element insertion
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:256
- Data Source:KIDDLAB
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: 201 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 201 SVs from 47 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3070456 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 6,798,218 | 6,798,473 |
| nsv3070456 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 6,907,384 | 6,907,639 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14040702 | mobile element insertion | SI000713L | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14040702 | Remapped | Perfect | NC_000012.12:g.679 8218_6798473ins? | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 6,798,218 | 6,798,473 |
| nssv14040702 | Submitted genomic | NC_000012.11:g.690 7384_6907639ins? | GRCh37 (hg19) | NC_000012.11 | Chr12 | 6,907,384 | 6,907,639 |