nsv4706002
- Organism: Homo sapiens
- Study:nstd195 (Mwapagha et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Mwapagha 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: 178 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 178 SVs from 39 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4706002 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 79,116,390 | 79,116,390 |
nsv4706002 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 79,582,075 | 79,582,075 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
nssv16247906 | insertion | B450 | Sequencing | Paired-end mapping | 1 | 4,473 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16247906 | Remapped | Perfect | NC_000001.11:g.791 16390_79116391ins3 08 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 79,116,390 | 79,116,390 |
nssv16247906 | Submitted genomic | NC_000001.10:g.795 82075_79582076ins3 08 | GRCh37 (hg19) | NC_000001.10 | Chr1 | 79,582,075 | 79,582,075 |