nsv5266432
- 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:3,500
- 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: 204 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 208 SVs from 50 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5266432 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000011.10 | Chr11 | 55,932,893 | 55,936,392 | ||
nsv5266432 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 55,700,369 | 55,703,868 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16757489 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv16757489 | Submitted genomic | GRCh38.p13 | NC_000011.10 | Chr11 | 55,932,893 | 55,936,392 | ||
nssv16757489 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 55,700,369 | 55,703,868 |