nsv4372237
- 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:26,007
- 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: 215 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 215 SVs from 53 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4372237 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 72,136,182 | 72,162,188 |
| nsv4372237 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 71,847,228 | 71,873,232 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15626477 | Remapped | Good | NC_000011.10:g.(?_ 72136182)_(7216218 8_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 72,136,182 | 72,162,188 |
| nssv15626539 | Remapped | Good | NC_000011.10:g.(?_ 72136182)_(7216218 8_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 72,136,182 | 72,162,188 |
| nssv15626477 | Submitted genomic | NC_000011.9:g.(?_7 1847228)_(71873232 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 71,847,228 | 71,873,232 | ||
| nssv15626539 | Submitted genomic | NC_000011.9:g.(?_7 1847228)_(71873232 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 71,847,228 | 71,873,232 |