Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv5555901 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000002.12 | Chr2 | 43,981,271 | 43,981,271 |
| nsv5555901 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 44,208,410 | 44,208,410 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv16913570 | sequence alteration | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv16913570 | Submitted genomic | | GRCh38 (hg38) | | NC_000002.12 | Chr2 | 43,981,271 | 43,981,271 |
| nssv16913570 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 44,208,410 | 44,208,410 |
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) |
|---|
| nssv16913570 | 0.017 | 106 | 6404 |
