nsv7058992
- 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:3,070,096
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: 8098 SVs from 100 studies. See in: genome view
Overlapping variant regions from other studies: 7261 SVs from 99 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7058992 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000014.9 | Chr14 | 90,104,468 | 93,174,563 | ||
| nsv7058992 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 90,570,812 | 93,372,264 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18755311 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18755311 | Submitted genomic | NC_000014.9:g.9010 4468_93174563inv | GRCh38 (hg38) | NC_000014.9 | Chr14 | 90,104,468 | 93,174,563 | ||
| nssv18755311 | Remapped | Pass | NC_000014.8:g.9057 0812_93372264inv | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 90,570,812 | 93,372,264 |
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) |
|---|---|---|---|
| nssv18755311 | 7e-06 | 2 | 276266 |