nsv4372211
- 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:94,758
- 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: 1029 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 1211 SVs from 71 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4372211 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 54,742,317 | 54,837,074 |
| nsv4372211 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 51,282,206 | 51,376,963 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15661848 | Remapped | Perfect | NC_000011.10:g.(?_ 54742317)_(5483707 4_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 54,742,317 | 54,837,074 |
| nssv15702258 | Remapped | Perfect | NC_000011.10:g.(?_ 54742317)_(5483707 4_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 54,742,317 | 54,837,074 |
| nssv15661848 | Submitted genomic | NC_000011.9:g.(?_5 1282206)_(51376963 _?)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 51,282,206 | 51,376,963 | ||
| nssv15702258 | Submitted genomic | NC_000011.9:g.(?_5 1282206)_(51376963 _?)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 51,282,206 | 51,376,963 |