nsv5329246
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:mobile element deletion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,095
- 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: 155 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 155 SVs from 56 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5329246 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000005.10 | Chr5 | 58,384,174 | 58,390,268 | ||
nsv5329246 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 57,680,001 | 57,686,095 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16769687 | line1 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 |
---|---|---|---|---|---|---|---|---|---|
nssv16769687 | Submitted genomic | NC_000005.10:g.583 84174_58390268del | GRCh38.p13 | NC_000005.10 | Chr5 | 58,384,174 | 58,390,268 | ||
nssv16769687 | Remapped | Perfect | NC_000005.9:g.5768 0001_57686095del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 57,680,001 | 57,686,095 |
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) |
---|---|
nssv16769687 | 0.901 |