Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|
| nsv5451362 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000003.12 | Chr3 | 48,491,970 | 48,496,165 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv16933733 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
|---|
| nssv16933733 | Submitted genomic | NC_000003.12:g.484
91970_48496165del | GRCh38 (hg38) | NC_000003.12 | Chr3 | 48,491,970 | 48,496,165 |
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) |
|---|
| nssv16933733 | 0.097 | 618 | 6394 |
