Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv4332896 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 42,500,295 | 42,650,077 |
| nsv4332896 | Submitted genomic | | GRCh37.p13 | Primary Assembly | | NC_000014.8 | Chr14 | 42,969,498 | 43,119,280 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv15788122 | sequence alteration | Sequencing | Other |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv15788122 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 42,500,295 | 42,650,077 |
| nssv15788122 | Submitted genomic | | GRCh37.p13 | | NC_000014.8 | Chr14 | 42,969,498 | 43,119,280 |
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) |
|---|
| nssv15788122 | <0.001 | 10 | 21694 |
