Genome View
Select assembly:Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nsv5432807 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000015.10 | Chr15 | 74,068,712 | 74,089,100 |
nsv5432807 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 74,361,053 | 74,381,441 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|
nssv17701057 | copy number variation | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nssv17701057 | Submitted genomic | | GRCh38 (hg38) | | NC_000015.10 | Chr15 | 74,068,712 | 74,089,100 |
nssv17701057 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 74,361,053 | 74,381,441 |
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) |
---|
nssv17701057 | 0.495 | 3029 | 6118 |