Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv5560956 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000004.12 | Chr4 | 68,883,815 | 69,126,528 |
| nsv5560956 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 69,749,533 | 69,992,246 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv16950549 | sequence alteration | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv16950549 | Submitted genomic | | GRCh38 (hg38) | | NC_000004.12 | Chr4 | 68,883,815 | 69,126,528 |
| nssv16950549 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 69,749,533 | 69,992,246 |
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) |
|---|
| nssv16950549 | 0.04 | 257 | 6404 |
