nsv4380747
- 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:47,315
- 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: 264 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 264 SVs from 47 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4380747 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 28,544,675 | 28,591,989 |
| nsv4380747 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 28,697,608 | 28,744,922 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15616675 | Remapped | Perfect | NC_000012.12:g.(?_ 28544675)_(2859198 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 28,544,675 | 28,591,989 |
| nssv15669828 | Remapped | Perfect | NC_000012.12:g.(?_ 28544675)_(2859198 9_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 28,544,675 | 28,591,989 |
| nssv15616675 | Submitted genomic | NC_000012.11:g.(?_ 28697608)_(2874492 2_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 28,697,608 | 28,744,922 | ||
| nssv15669828 | Submitted genomic | NC_000012.11:g.(?_ 28697608)_(2874492 2_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 28,697,608 | 28,744,922 |