Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv5561628 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000012.12 | Chr12 | 110,480,278 | 110,483,266 |
| nsv5561628 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 110,918,083 | 110,921,071 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv17684428 | sequence alteration | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv17684428 | Submitted genomic | | GRCh38 (hg38) | | NC_000012.12 | Chr12 | 110,480,278 | 110,483,266 |
| nssv17684428 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 110,918,083 | 110,921,071 |
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) |
|---|
| nssv17684428 | 0.004 | 26 | 6404 |
