Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv4319221 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 20,754,592 | 20,756,191 |
| nsv4319221 | Submitted genomic | | GRCh37.p13 | Primary Assembly | | NC_000024.9 | ChrY | 22,916,478 | 22,918,077 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv15791835 | sequence alteration | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv15791835 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 20,754,592 | 20,756,191 |
| nssv15791835 | Submitted genomic | | GRCh37.p13 | | NC_000024.9 | ChrY | 22,916,478 | 22,918,077 |
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) |
|---|
| nssv15791835 | <0.001 | 2 | 11056 |
