nsv5221318
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:85,900
- Publication(s):Chen 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: 284 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 284 SVs from 45 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5221318 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000003.12 | Chr3 | 113,388,101 | 113,474,000 | ||
nsv5221318 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 113,106,948 | 113,192,847 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16842206 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv16842206 | Submitted genomic | GRCh38.p13 | NC_000003.12 | Chr3 | 113,388,101 | 113,474,000 | ||
nssv16842206 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 113,106,948 | 113,192,847 |