nsv5879193
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,643
- Publication(s):Almarri et al. 2020
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: 255 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 255 SVs from 43 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5879193 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000017.11 | Chr17 | 30,738,213 | 30,739,855 | ||
nsv5879193 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 29,065,231 | 29,066,873 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Copy number |
---|---|---|---|---|
nssv17473074 | copy number variation | Sequencing | Sequence alignment | 2 |
nssv17477586 | copy number variation | Sequencing | Sequence alignment | 0 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv17473074 | Submitted genomic | GRCh38 (hg38) | NC_000017.11 | Chr17 | 30,738,213 | 30,739,855 | ||
nssv17477586 | Submitted genomic | GRCh38 (hg38) | NC_000017.11 | Chr17 | 30,738,213 | 30,739,855 | ||
nssv17473074 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 29,065,231 | 29,066,873 |
nssv17477586 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 29,065,231 | 29,066,873 |