Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|
| nsv5558534 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000022.11 | Chr22 | 11,285,958 | 11,597,527 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv17727374 | sequence alteration | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Assembly | Sequence ID | Chr | Start | Stop |
|---|
| nssv17727374 | Submitted genomic | GRCh38 (hg38) | NC_000022.11 | Chr22 | 11,285,958 | 11,597,527 |
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) |
|---|
| nssv17727374 | 0.004 | 27 | 6404 |
