Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|
| nsv7072143 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 2,582,010 | 2,640,135 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv18783288 | inversion | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
|---|
| nssv18783288 | Submitted genomic | NC_000008.11:g.258
2010_2640135inv | GRCh38 (hg38) | NC_000008.11 | Chr8 | 2,582,010 | 2,640,135 |
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) |
|---|
| nssv18783288 | <0.001 | 35 | 274776 |
