nsv5415625
- 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:1,621
- 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: 106 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 112 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5415625 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 156,896,468 (-50, +242) | 156,898,088 (-241, +49) | ||
| nsv5415625 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 156,866,260 (-50, +242) | 156,867,880 (-241, +49) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16890935 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16890935 | Submitted genomic | NC_000001.11:g.(15 6896418_156896710) _(156897847_156898 137)del | GRCh38 (hg38) | NC_000001.11 | Chr1 | 156,896,468 (-50, +242) | 156,898,088 (-241, +49) | ||
| nssv16890935 | Remapped | Perfect | NC_000001.10:g.(15 6866210_156866502) _(156867639_156867 929)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 156,866,260 (-50, +242) | 156,867,880 (-241, +49) |
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) |
|---|---|---|---|
| nssv16890935 | <0.001 | 1 | 6404 |