nsv5485289
- Organism: Homo sapiens
- Study:nstd206 (Byrska-Bishop et al. 2022)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:923
- Publication(s):Byrska-Bishop et al. 2022
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: 87 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 24 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5485289 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 125,225,671 | 125,226,593 | ||
nsv5485289 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 127,987,950 | 127,988,872 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17028673 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17028673 | Submitted genomic | NC_000009.12:g.125 225671_125226593de l | GRCh38 (hg38) | NC_000009.12 | Chr9 | 125,225,671 | 125,226,593 | ||
nssv17028673 | Remapped | Perfect | NC_000009.11:g.127 987950_127988872de l | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 127,987,950 | 127,988,872 |
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) |
---|---|---|---|
nssv17028673 | 0.003 | 19 | 6402 |