nsv4377466
- 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:2,772,256
- 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: 11161 SVs from 135 studies. See in: genome view
Overlapping variant regions from other studies: 10208 SVs from 132 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4377466 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 18,339,130 | 21,111,385 |
| nsv4377466 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 18,916,843 | 21,465,674 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15656509 | Remapped | Pass | NC_000022.11:g.(?_ 18339130)_(2111138 5_?)dup | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 18,339,130 | 21,111,385 |
| nssv15670182 | Remapped | Pass | NC_000022.11:g.(?_ 18339130)_(2111138 5_?)dup | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 18,339,130 | 21,111,385 |
| nssv15656509 | Submitted genomic | NC_000022.10:g.(?_ 18916843)_(2146567 4_?)dup | GRCh37 (hg19) | NC_000022.10 | Chr22 | 18,916,843 | 21,465,674 | ||
| nssv15670182 | Submitted genomic | NC_000022.10:g.(?_ 18916843)_(2146567 4_?)dup | GRCh37 (hg19) | NC_000022.10 | Chr22 | 18,916,843 | 21,465,674 |