nsv6621349
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:158,010
- Publication(s):Zarrei et al. 2023
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: 2041 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 2041 SVs from 80 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6621349 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 37,566,333 | 37,724,342 |
| nsv6621349 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 37,960,135 | 38,118,144 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18309305 | duplication | OSC7112 | SNP array | Probe signal intensity | 10 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18309305 | Remapped | Perfect | NC_000012.12:g.(?_ 37566333)_(3772434 2_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 37,566,333 | 37,724,342 |
| nssv18309305 | Submitted genomic | NC_000012.11:g.(?_ 37960135)_(3811814 4_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 37,960,135 | 38,118,144 |