nsv5835822
- 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:1,050
- 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: 211 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 211 SVs from 52 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5835822 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000003.12 | Chr3 | 198,117,445 | 198,118,494 | ||
| nsv5835822 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 197,844,316 | 197,845,365 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Copy number |
|---|---|---|---|---|
| nssv17489938 | copy number variation | Sequencing | Sequence alignment | 0 |
| nssv17490150 | copy number variation | Sequencing | Sequence alignment | 2 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv17489938 | Submitted genomic | GRCh38 (hg38) | NC_000003.12 | Chr3 | 198,117,445 | 198,118,494 | ||
| nssv17490150 | Submitted genomic | GRCh38 (hg38) | NC_000003.12 | Chr3 | 198,117,445 | 198,118,494 | ||
| nssv17489938 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 197,844,316 | 197,845,365 |
| nssv17490150 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 197,844,316 | 197,845,365 |