nsv3401003
- Organism: Homo sapiens
- Study:nstd162 (Audano et al. 2019)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Audano et al. 2019
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: 367 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 367 SVs from 60 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3401003 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 150,038,857 | 150,038,857 | ||
| nsv3401003 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 149,735,946 | 149,735,946 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14761204 | herv insertion | SAMN04229552 | Sequencing | de novo and local sequence assembly | 24,632 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14761204 | Submitted genomic | NC_000007.14:g.150 038857_150038858in s1968 | GRCh38 (hg38) | NC_000007.14 | Chr7 | 150,038,857 | 150,038,857 | ||
| nssv14761204 | Remapped | Perfect | NC_000007.13:g.149 735946_149735947in s1968NC_000007.13: g.149735946_149735 947ins1968 | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 149,735,946 | 149,735,946 |