nsv7073751
- Organism: Homo sapiens
- Study:nstd229 (Jun et al. 2023)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:720,458
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: 2414 SVs from 112 studies. See in: genome view
Overlapping variant regions from other studies: 2387 SVs from 112 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv7073751 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 49,459,138 | 50,179,595 | ||
nsv7073751 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 49,480,690 | 50,138,766 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18736486 | inversion | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18736486 | Submitted genomic | NC_000011.10:g.494 59138_50179595inv | GRCh38 (hg38) | NC_000011.10 | Chr11 | 49,459,138 | 50,179,595 | ||
nssv18736486 | Remapped | Pass | NC_000011.9:g.4948 0690_50138766inv | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 49,480,690 | 50,138,766 |
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) | Allele Count (AC) | Allele Number (AN) |
---|---|---|---|
nssv18736486 | 1.1e-05 | 3 | 274320 |