nsv5563808
- Organism: Homo sapiens
- Study:nstd206 (Byrska-Bishop et al. 2022)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:847
- Publication(s):Byrska-Bishop et al. 2022
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: 106 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 106 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5563808 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000003.12 | Chr3 | 125,018,878 (-42, +125) | 125,019,724 (-64, +43) | ||
| nsv5563808 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 124,737,722 (-42, +125) | 124,738,568 (-64, +43) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16938165 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16938165 | Submitted genomic | NC_000003.12:g.(12 5018836_125019003) _(125019660_125019 767)inv | GRCh38 (hg38) | NC_000003.12 | Chr3 | 125,018,878 (-42, +125) | 125,019,724 (-64, +43) | ||
| nssv16938165 | Remapped | Perfect | NC_000003.11:g.(12 4737680_124737847) _(124738504_124738 611)inv | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 124,737,722 (-42, +125) | 124,738,568 (-64, +43) |
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) |
|---|---|---|---|
| nssv16938165 | <0.001 | 2 | 6404 |