nsv4329748
- 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:6,609,007
- 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: 4960 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 4960 SVs from 25 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4329748 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 11,255,910 | 17,864,916 |
| nsv4329748 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000012.11 | Chr12 | 11,408,826 | 18,017,850 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16090775 | inversion | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16090775 | Remapped | Perfect | NC_000012.12:g.112 55910_17864916inv | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 11,255,910 | 17,864,916 |
| nssv16090775 | Submitted genomic | NC_000012.11:g.114 08826_18017850inv | GRCh37.p13 | NC_000012.11 | Chr12 | 11,408,826 | 18,017,850 |
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) |
|---|---|---|---|
| nssv16090775 | 4.6e-005 | 1 | 21692 |