nsv5554140
- 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:94,507
- 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: 269 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 269 SVs from 39 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5554140 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000004.12 | Chr4 | 18,175,371 (-28) | 18,269,877 (-38, +27) | ||
| nsv5554140 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 18,176,994 (-28) | 18,271,500 (-38, +27) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16948329 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16948329 | Submitted genomic | NC_000004.12:g.(18 175343_?)_(1826983 9_18269904)inv | GRCh38 (hg38) | NC_000004.12 | Chr4 | 18,175,371 (-28) | 18,269,877 (-38, +27) | ||
| nssv16948329 | Remapped | Perfect | NC_000004.11:g.(18 176966_?)_(1827146 2_18271527)inv | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 18,176,994 (-28) | 18,271,500 (-38, +27) |
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) |
|---|---|---|---|
| nssv16948329 | 0.459 | 2940 | 6404 |