Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv5556707 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000009.12 | Chr9 | 126,660,074 | 126,660,074 |
| nsv5556707 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 129,422,353 | 129,422,353 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv17028715 | sequence alteration | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv17028715 | Submitted genomic | | GRCh38 (hg38) | | NC_000009.12 | Chr9 | 126,660,074 | 126,660,074 |
| nssv17028715 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 129,422,353 | 129,422,353 |
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) |
|---|
| nssv17028715 | 0.24 | 1540 | 6404 |
