Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|
| nsv7037768 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000021.9 | Chr21 | 7,919,387 | 10,699,868 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv18438468 | deletion | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
|---|
| nssv18438468 | Submitted genomic | NC_000021.9:g.7919
387_10699868del | GRCh38 (hg38) | NC_000021.9 | Chr21 | 7,919,387 | 10,699,868 |
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) |
|---|
| nssv18438468 | 1 | 264292 | 264338 |
