nsv6246205
- Organism: Homo sapiens
- Study:nstd215 (Prakrithi et al. 2022)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Prakrithi et al. 2022
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: 145 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 145 SVs from 19 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6246205 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 79,852,656 | 79,852,656 | ||
nsv6246205 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 80,764,891 | 80,764,891 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17839929 | alu insertion | Sequencing | Split read mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17839929 | Submitted genomic | NC_000008.11:g.798 52656_79852657ins2 81 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 79,852,656 | 79,852,656 | ||
nssv17839929 | Remapped | Perfect | NC_000008.10:g.807 64891_80764892ins2 81 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 80,764,891 | 80,764,891 |