nsv5652087
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Ebert 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: 265 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 260 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 24 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5652087 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000019.10 | Chr19 | 20,198,932 | 20,198,932 | ||
| nsv5652087 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000019.9 | Chr19 | 20,309,741 | 20,309,741 |
| nsv5652087 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003571053.2 | Chr19|NW_0 03571053.2 | 116,185 | 116,185 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17103931 | Submitted genomic | NC_000019.10:g.201 98932_20198933ins3 20 | GRCh38 (hg38) | NC_000019.10 | Chr19 | 20,198,932 | 20,198,932 | ||
| nssv17103931 | Remapped | Perfect | NW_003571053.2:g.1 16185_116186ins320 | GRCh37.p13 | First Pass | NW_003571053.2 | Chr19|NW_0 03571053.2 | 116,185 | 116,185 |
| nssv17103931 | Remapped | Perfect | NC_000019.9:g.2030 9741_20309742ins32 0 | GRCh37.p13 | Second Pass | NC_000019.9 | Chr19 | 20,309,741 | 20,309,741 |