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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nsv3067127 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 44,455 | 231,326 |
nsv3067127 | Submitted genomic | | GRCh37 (hg19) | Primary Assembly | | NC_000016.9 | Chr16 | 94,455 | 281,325 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|
nssv14038740 | complex substitution | Sequencing | Read depth and paired-end mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|
nssv14038740 | Remapped | Good | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 44,455 | 231,326 |
nssv14038740 | Submitted genomic | | GRCh37 (hg19) | | NC_000016.9 | Chr16 | 94,455 | 281,325 |
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) |
---|
nssv14038740 | 4.49e-005 |