nsv5704928
- 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 Alu 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: 102 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 102 SVs from 25 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5704928 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 43,794,667 | 43,794,667 | ||
nsv5704928 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 43,816,217 | 43,816,217 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17191164 | alu insertion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17191164 | Submitted genomic | NC_000011.10:g.437 94667_43794668ins2 80 | GRCh38 (hg38) | NC_000011.10 | Chr11 | 43,794,667 | 43,794,667 | ||
nssv17191164 | Remapped | Perfect | NC_000011.9:g.4381 6217_43816218ins28 0 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 43,816,217 | 43,816,217 |