nsv4379390
- 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:21,616
- 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: 430 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 430 SVs from 63 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4379390 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 232,384,546 | 232,406,161 |
| nsv4379390 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 233,249,256 | 233,270,871 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15613702 | Remapped | Perfect | NC_000002.12:g.(?_ 232384546)_(232406 161_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 232,384,546 | 232,406,161 |
| nssv15688466 | Remapped | Perfect | NC_000002.12:g.(?_ 232384546)_(232406 161_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 232,384,546 | 232,406,161 |
| nssv15613702 | Submitted genomic | NC_000002.11:g.(?_ 233249256)_(233270 871_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 233,249,256 | 233,270,871 | ||
| nssv15688466 | Submitted genomic | NC_000002.11:g.(?_ 233249256)_(233270 871_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 233,249,256 | 233,270,871 |