nsv4320793
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:30,882
- Publication(s):gnomAD_Structural_Variants
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: 66 SVs from 10 studies. See in: genome view
Overlapping variant regions from other studies: 66 SVs from 10 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4320793 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 133,941,717 | 133,972,598 |
nsv4320793 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000004.11 | Chr4 | 134,862,872 | 134,893,753 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16091330 | inversion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16091330 | Remapped | Perfect | NC_000004.12:g.133 941717_133972598in v | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 133,941,717 | 133,972,598 |
nssv16091330 | Submitted genomic | NC_000004.11:g.134 862872_134893753in v | GRCh37.p13 | NC_000004.11 | Chr4 | 134,862,872 | 134,893,753 |
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) |
---|---|---|---|
nssv16091330 | 4.6e-005 | 1 | 21694 |