nsv5625030
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- 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: 333 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 333 SVs from 32 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5625030 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 17,883,306 | 17,883,306 | ||
| nsv5625030 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 17,740,815 | 17,740,815 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17140898 | Submitted genomic | NC_000008.11:g.178 83306_17883307ins7 1 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 17,883,306 | 17,883,306 | ||
| nssv17157134 | Submitted genomic | NC_000008.11:g.178 83306_17883307ins2 11 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 17,883,306 | 17,883,306 | ||
| nssv17140898 | Remapped | Perfect | NC_000008.10:g.177 40815_17740816ins7 1 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 17,740,815 | 17,740,815 |
| nssv17157134 | Remapped | Perfect | NC_000008.10:g.177 40815_17740816ins2 11 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 17,740,815 | 17,740,815 |