Genome View
Select assembly:Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
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nsv5562834 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000024.10 | ChrY | 19,066,442 | 19,177,974 |
nsv5562834 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 21,228,328 | 21,339,860 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|
nssv17742831 | sequence alteration | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nssv17742831 | Submitted genomic | | GRCh38 (hg38) | | NC_000024.10 | ChrY | 19,066,442 | 19,177,974 |
nssv17742831 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 21,228,328 | 21,339,860 |
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) |
---|
nssv17742831 | <0.001 | 2 | 3198 |