Genome View
Select assembly:Variant Region Placement Information
Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
---|
nsv5977042 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 1,189,309 | 1,194,478 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Copy number |
---|
nssv17515241 | copy number variation | Sequencing | Sequence alignment | 2 |
Variant Call Placement Information
Variant Call ID | Placement Type | Assembly | Sequence ID | Chr | Start | Stop |
---|
nssv17515241 | Submitted genomic | GRCh38 (hg38) | NC_000023.11 | ChrX | 1,189,309 | 1,194,478 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype and/or allele frequency data can be found on dbVar's FTP site.