nsv5554795
- 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:66,156
- 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: 241 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 241 SVs from 40 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5554795 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000003.12 | Chr3 | 154,997,783 (-136, +341) | 155,063,938 (-70, +331) | ||
| nsv5554795 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 154,715,572 (-136, +341) | 154,781,727 (-70, +331) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16941894 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16941894 | Submitted genomic | NC_000003.12:g.(15 4997647_154998124) _(155063868_155064 269)inv | GRCh38 (hg38) | NC_000003.12 | Chr3 | 154,997,783 (-136, +341) | 155,063,938 (-70, +331) | ||
| nssv16941894 | Remapped | Perfect | NC_000003.11:g.(15 4715436_154715913) _(154781657_154782 058)inv | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 154,715,572 (-136, +341) | 154,781,727 (-70, +331) |
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) |
|---|---|---|---|
| nssv16941894 | <0.001 | 6 | 6404 |