Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv4339288 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 123,021,058 | 123,176,398 |
| nsv4339288 | Submitted genomic | | GRCh37.p13 | Primary Assembly | | NC_000002.11 | Chr2 | 123,778,634 | 123,933,974 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv15789599 | sequence alteration | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv15789599 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 123,021,058 | 123,176,398 |
| nssv15789599 | Submitted genomic | | GRCh37.p13 | | NC_000002.11 | Chr2 | 123,778,634 | 123,933,974 |
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) |
|---|
| nssv15789599 | <0.001 | 3 | 21694 |
