nsv5471148
- 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:286,411
- 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: 711 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 711 SVs from 54 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5471148 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 108,077,448 (-22, +20) | 108,363,858 (-20, +22) | ||
| nsv5471148 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 107,413,149 (-22, +20) | 107,699,559 (-20, +22) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16972626 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16972626 | Submitted genomic | NC_000005.10:g.(10 8077426_108077468) _(108363838_108363 880)del | GRCh38 (hg38) | NC_000005.10 | Chr5 | 108,077,448 (-22, +20) | 108,363,858 (-20, +22) | ||
| nssv16972626 | Remapped | Perfect | NC_000005.9:g.(107 413127_107413169)_ (107699539_1076995 81)del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 107,413,149 (-22, +20) | 107,699,559 (-20, +22) |
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) |
|---|---|---|---|
| nssv16972626 | <0.001 | 1 | 6404 |