nsv5205376
- 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:322
- 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: 180 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 180 SVs from 58 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5205376 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000012.12 | Chr12 | 122,525,799 | 122,526,120 | ||
nsv5205376 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 123,010,346 | 123,010,667 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16741823 | alu 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 |
---|---|---|---|---|---|---|---|---|---|
nssv16741823 | Submitted genomic | NC_000012.12:g.122 525799_122526120de l | GRCh38.p13 | NC_000012.12 | Chr12 | 122,525,799 | 122,526,120 | ||
nssv16741823 | Remapped | Perfect | NC_000012.11:g.123 010346_123010667de l | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 123,010,346 | 123,010,667 |
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) |
---|---|
nssv16741823 | 0.783 |