nsv5719366
- Organism: Homo sapiens
- Study:nstd211 (Chuang et al. 2021)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Description:Insertion of a HERV mobile element relative to the reference
- Publication(s):Chuang et al. 2021
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: 157 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5719366 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000013.11 | Chr13 | 38,838,267 | 38,838,267 | ||
nsv5719366 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 39,412,404 | 39,412,404 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17222694 | herv insertion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17222694 | Submitted genomic | NC_000013.11:g.388 38267_38838268ins8 399 | GRCh38 (hg38) | NC_000013.11 | Chr13 | 38,838,267 | 38,838,267 | ||
nssv17222694 | Remapped | Perfect | NC_000013.10:g.394 12404_39412405ins8 399 | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 39,412,404 | 39,412,404 |