nsv5499369
- 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:959
- 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: 163 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 163 SVs from 45 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5499369 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000012.12 | Chr12 | 109,661,306 (-264, +69) | 109,662,264 (-60, +85) | ||
| nsv5499369 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 110,099,111 (-264, +69) | 110,100,069 (-60, +85) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17684380 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17684380 | Submitted genomic | NC_000012.12:g.(10 9661042_109661375) _(109662204_109662 349)dup | GRCh38 (hg38) | NC_000012.12 | Chr12 | 109,661,306 (-264, +69) | 109,662,264 (-60, +85) | ||
| nssv17684380 | Remapped | Perfect | NC_000012.11:g.(11 0098847_110099180) _(110100009_110100 154)dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 110,099,111 (-264, +69) | 110,100,069 (-60, +85) |
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) |
|---|---|---|---|
| nssv17684380 | 0.949 | 6076 | 6404 |