nsv4381107
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:45,436
- Publication(s):Zarrei et al. 2019
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: 266 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 266 SVs from 61 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4381107 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 56,938,290 | 56,983,725 |
| nsv4381107 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 57,332,074 | 57,377,509 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15619562 | Remapped | Perfect | NC_000012.12:g.(?_ 56938290)_(5698372 5_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 56,938,290 | 56,983,725 |
| nssv15642530 | Remapped | Perfect | NC_000012.12:g.(?_ 56938290)_(5698372 5_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 56,938,290 | 56,983,725 |
| nssv15619562 | Submitted genomic | NC_000012.11:g.(?_ 57332074)_(5737750 9_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 57,332,074 | 57,377,509 | ||
| nssv15642530 | Submitted genomic | NC_000012.11:g.(?_ 57332074)_(5737750 9_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 57,332,074 | 57,377,509 |