nsv4378194
- 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:47,772
- 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: 594 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 595 SVs from 56 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4378194 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 104,002,981 | 104,050,752 |
| nsv4378194 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 103,257,553 | 103,305,318 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15630907 | Remapped | Good | NC_000023.11:g.(?_ 104002981)_(104050 752_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 104,002,981 | 104,050,752 |
| nssv15690926 | Remapped | Good | NC_000023.11:g.(?_ 104002981)_(104050 752_?)dup | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 104,002,981 | 104,050,752 |
| nssv15630907 | Submitted genomic | NC_000023.10:g.(?_ 103257553)_(103305 318_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 103,257,553 | 103,305,318 | ||
| nssv15690926 | Submitted genomic | NC_000023.10:g.(?_ 103257553)_(103305 318_?)dup | GRCh37 (hg19) | NC_000023.10 | ChrX | 103,257,553 | 103,305,318 |