nsv7085992
- Organism: Homo sapiens
- Study:nstd229 (Jun et al. 2023)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:89,500
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 421 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 422 SVs from 36 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv7085992 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 18,606,901 | 18,696,400 | ||
nsv7085992 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 18,625,021 | 18,714,519 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18656609 | duplication | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18656609 | Submitted genomic | NC_000023.11:g.186 06901_18696400dup | GRCh38 (hg38) | NC_000023.11 | ChrX | 18,606,901 | 18,696,400 | ||
nssv18656609 | Remapped | Good | NC_000023.10:g.186 25021_18714519dup | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 18,625,021 | 18,714,519 |
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) |
---|---|---|---|
nssv18656609 | 5e-06 | 1 | 200000 |