nsv5980318
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Almarri et al. 2020
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: 252 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 69 SVs from 17 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5980318 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000017.11 | Chr17 | 81,432,557 | 81,432,557 | ||
| nsv5980318 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871087.1 | Chr17|NW_0 03871087.1 | 87,195 | 87,195 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17382643 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17382643 | Submitted genomic | NC_000017.11:g.814 32557_81432558ins6 8 | GRCh38 (hg38) | NC_000017.11 | Chr17 | 81,432,557 | 81,432,557 | ||
| nssv17382643 | Remapped | Perfect | NW_003871087.1:g.8 7195_87196ins68 | GRCh37.p13 | First Pass | NW_003871087.1 | Chr17|NW_0 03871087.1 | 87,195 | 87,195 |