nsv5513712
- 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:1,031
- 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: 138 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 138 SVs from 42 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5513712 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000012.12 | Chr12 | 49,878,271 (-70, +162) | 49,879,301 (-41, +55) | ||
| nsv5513712 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 50,272,054 (-70, +162) | 50,273,084 (-41, +55) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17056420 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17056420 | Submitted genomic | NC_000012.12:g.(49 878201_49878433)_( 49879260_49879356) del | GRCh38 (hg38) | NC_000012.12 | Chr12 | 49,878,271 (-70, +162) | 49,879,301 (-41, +55) | ||
| nssv17056420 | Remapped | Perfect | NC_000012.11:g.(50 271984_50272216)_( 50273043_50273139) del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 50,272,054 (-70, +162) | 50,273,084 (-41, +55) |
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) |
|---|---|---|---|
| nssv17056420 | 0.337 | 2160 | 6402 |