Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv4344500 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 89,771,606 | 89,857,148 |
| nsv4344500 | Submitted genomic | | GRCh37.p13 | Primary Assembly | | NC_000015.9 | Chr15 | 90,314,837 | 90,400,380 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv15788310 | sequence alteration | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv15788310 | Remapped | Good | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 89,771,606 | 89,857,148 |
| nssv15788310 | Submitted genomic | | GRCh37.p13 | | NC_000015.9 | Chr15 | 90,314,837 | 90,400,380 |
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) |
|---|
| nssv15788310 | 4.6e-005 | 1 | 21692 |
