nsv4768286
- Organism: Homo sapiens
- Study:nstd199 (Quan et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Quan 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: 129 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 129 SVs from 21 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4768286 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 66,336,672 | 66,336,672 |
nsv4768286 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 64,332,790 | 64,332,790 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16269535 | insertion | Sequencing | Split read mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16269535 | Remapped | Perfect | NC_000017.11:g.663 36672_66336673ins5 4 | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 66,336,672 | 66,336,672 |
nssv16269535 | Submitted genomic | NC_000017.10:g.643 32790_64332791ins5 4 | GRCh37 (hg19) | NC_000017.10 | Chr17 | 64,332,790 | 64,332,790 |