Genome View
Select assembly:Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nsv5415118 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000001.11 | Chr1 | 155,213,250 | 155,234,587 |
| nsv5415118 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 155,183,041 | 155,204,378 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|
| nssv16890439 | copy number variation | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|
| nssv16890439 | Submitted genomic | | GRCh38 (hg38) | | NC_000001.11 | Chr1 | 155,213,250 | 155,234,587 |
| nssv16890439 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 155,183,041 | 155,204,378 |
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) |
|---|
| nssv16890439 | 0.063 | 131 | 2078 |
