Genome View
Select assembly:Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nsv4662604 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 18,924,644 | 19,011,486 |
nsv4662604 | Submitted genomic | | GRCh37 (hg19) | Primary Assembly | | NC_000022.10 | Chr22 | 18,912,157 | 18,998,999 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|
nssv16206024 | copy number variation | Curated | Curated |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nssv16206024 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 18,924,644 | 19,011,486 |
nssv16206024 | Submitted genomic | | GRCh37 (hg19) | | NC_000022.10 | Chr22 | 18,912,157 | 18,998,999 |
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) |
---|
nssv16206024 | 0.014 | 69 | 5008 |