nsv7079896
- 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:30,900
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: 420 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 414 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 69 SVs from 27 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7079896 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 154,376,201 | 154,407,100 | ||
| nsv7079896 | Remapped | Good | GRCh37.p13 | Primary Assembly | Second Pass | NC_000023.10 | ChrX | 153,604,561 | 153,635,441 |
| nsv7079896 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871103.3 | ChrX|NW_00 3871103.3 | 1,810,180 | 1,841,079 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18455143 | deletion | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv18455143 | Submitted genomic | NC_000023.11:g.154 376201_154407100de l | GRCh38 (hg38) | NC_000023.11 | ChrX | 154,376,201 | 154,407,100 | ||
| nssv18455143 | Remapped | Perfect | NW_003871103.3:g.1 810180_1841079del | GRCh37.p13 | First Pass | NW_003871103.3 | ChrX|NW_00 3871103.3 | 1,810,180 | 1,841,079 |
| nssv18455143 | Remapped | Good | NC_000023.10:g.153 604561_153635441de l | GRCh37.p13 | Second Pass | NC_000023.10 | ChrX | 153,604,561 | 153,635,441 |
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) |
|---|---|---|---|
| nssv18455143 | 5e-06 | 1 | 200000 |