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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nsv5428476 | Submitted genomic | | GRCh38 (hg38) | Primary Assembly | | NC_000001.11 | Chr1 | 175,100,587 | 175,108,440 |
nsv5428476 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 175,069,723 | 175,077,576 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|
nssv16892261 | copy number variation | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nssv16892261 | Submitted genomic | | GRCh38 (hg38) | | NC_000001.11 | Chr1 | 175,100,587 | 175,108,440 |
nssv16892261 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 175,069,723 | 175,077,576 |
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) |
---|
nssv16892261 | 0.488 | 965 | 1978 |