Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv5558356 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000006.12 | Chr6 | 29,437,544 | 29,438,789 |
| nsv5558356 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 29,405,321 | 29,406,566 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv16982464 | sequence alteration | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv16982464 | Submitted genomic | | GRCh38 (hg38) | | NC_000006.12 | Chr6 | 29,437,544 | 29,438,789 |
| nssv16982464 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 29,405,321 | 29,406,566 |
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) |
|---|
| nssv16982464 | 0.053 | 340 | 6404 |
