Genome View
Select assembly:Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nsv4337678 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 56,179,749 | 56,589,194 |
nsv4337678 | Submitted genomic | | GRCh37.p13 | Primary Assembly | | NC_000004.11 | Chr4 | 57,045,915 | 57,455,360 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|
nssv15790195 | sequence alteration | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nssv15790195 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 56,179,749 | 56,589,194 |
nssv15790195 | Submitted genomic | | GRCh37.p13 | | NC_000004.11 | Chr4 | 57,045,915 | 57,455,360 |
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) |
---|
nssv15790195 | <0.001 | 13 | 21664 |