nsv5635685
- 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: 194 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 194 SVs from 26 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5635685 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 94,782,492 | 94,782,492 | ||
nsv5635685 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 95,794,720 | 95,794,720 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17144982 | Submitted genomic | NC_000008.11:g.947 82492_94782493ins3 15 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 94,782,492 | 94,782,492 | ||
nssv17144982 | Remapped | Perfect | NC_000008.10:g.957 94720_95794721ins3 15 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 95,794,720 | 95,794,720 |