Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv5563970 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000012.12 | Chr12 | 76,420,062 | 76,420,063 |
| nsv5563970 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 76,813,842 | 76,813,843 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv17689274 | sequence alteration | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv17689274 | Submitted genomic | | GRCh38 (hg38) | | NC_000012.12 | Chr12 | 76,420,062 | 76,420,063 |
| nssv17689274 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 76,813,842 | 76,813,843 |
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) |
|---|
| nssv17689274 | <0.001 | 2 | 6404 |
