nsv5283013
- 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:556
- 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: 609 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 609 SVs from 49 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5283013 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000001.11 | Chr1 | 2,211,645 (-12, +2) | 2,212,200 (-5, +20) | ||
| nsv5283013 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 2,143,084 (-12, +2) | 2,143,639 (-5, +20) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16742747 | duplication | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16742747 | Submitted genomic | NC_000001.11:g.(22 11633_2211647)_(22 12195_2212220)dup | GRCh38.p13 | NC_000001.11 | Chr1 | 2,211,645 (-12, +2) | 2,212,200 (-5, +20) | ||
| nssv16742747 | Remapped | Perfect | NC_000001.10:g.(21 43072_2143086)_(21 43634_2143659)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 2,143,084 (-12, +2) | 2,143,639 (-5, +20) |
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) |
|---|---|
| nssv16742747 | 0.286 |