nsv6621753
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:19,632
- 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: 426 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 426 SVs from 64 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6621753 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 8,222,150 | 8,241,781 |
| nsv6621753 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 8,374,746 | 8,394,377 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18301493 | Remapped | Perfect | NC_000012.12:g.(?_ 8222150)_(8241781_ ?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 8,222,150 | 8,241,781 |
| nssv18315976 | Remapped | Perfect | NC_000012.12:g.(?_ 8222150)_(8241781_ ?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 8,222,150 | 8,241,781 |
| nssv18301493 | Submitted genomic | NC_000012.11:g.(?_ 8374746)_(8394377_ ?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 8,374,746 | 8,394,377 | ||
| nssv18315976 | Submitted genomic | NC_000012.11:g.(?_ 8374746)_(8394377_ ?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 8,374,746 | 8,394,377 |