nsv5298869
- 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:4,718
- 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: 218 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 218 SVs from 42 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5298869 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000001.11 | Chr1 | 11,928,633 | 11,933,350 (-1) | ||
nsv5298869 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 11,988,690 | 11,993,407 (-1) |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16748520 | deletion | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16748520 | Submitted genomic | NC_000001.11:g.119 28633_(11933349_?) del | GRCh38.p13 | NC_000001.11 | Chr1 | 11,928,633 | 11,933,350 (-1) | ||
nssv16748520 | Remapped | Perfect | NC_000001.10:g.119 88690_(11993406_?) del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 11,988,690 | 11,993,407 (-1) |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
Variant Call ID | Allele Frequency (AF) |
---|---|
nssv16748520 | 0.031 |