nsv7055224
- 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:1,249,637
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: 2050 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 2007 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 818 SVs from 42 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7055224 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 149,372,897 | 150,622,533 | ||
| nsv7055224 | Remapped | Pass | GRCh37.p13 | Primary Assembly | Second Pass | NC_000023.10 | ChrX | 148,454,427 | 149,791,006 |
| nsv7055224 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_004070890.2 | ChrX|NW_00 4070890.2 | 4,897,294 | 6,146,931 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18763528 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18763528 | Submitted genomic | NC_000023.11:g.149 372897_150622533in v | GRCh38 (hg38) | NC_000023.11 | ChrX | 149,372,897 | 150,622,533 | ||
| nssv18763528 | Remapped | Perfect | NW_004070890.2:g.4 897294_6146931inv | GRCh37.p13 | First Pass | NW_004070890.2 | ChrX|NW_00 4070890.2 | 4,897,294 | 6,146,931 |
| nssv18763528 | Remapped | Pass | NC_000023.10:g.148 454427_149791006in v | GRCh37.p13 | Second Pass | NC_000023.10 | ChrX | 148,454,427 | 149,791,006 |
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) |
|---|---|---|---|
| nssv18763528 | 5e-06 | 1 | 200000 |