Genome View
Select assembly:Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nsv4659313 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 16,044,125 | 16,055,158 |
nsv4659313 | Submitted genomic | | GRCh37 (hg19) | Primary Assembly | | NC_000001.10 | Chr1 | 16,370,620 | 16,381,653 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|
nssv16206035 | copy number variation | Curated | Curated |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nssv16206035 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 16,044,125 | 16,055,158 |
nssv16206035 | Submitted genomic | | GRCh37 (hg19) | | NC_000001.10 | Chr1 | 16,370,620 | 16,381,653 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
---|
nssv16206035 | 0.011 | 57 | 5008 |