nsv6629424
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:59,588
- Publication(s):Zarrei et al. 2023
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: 250 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 250 SVs from 42 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6629424 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 22,713,407 | 22,772,994 |
| nsv6629424 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 22,715,030 | 22,774,617 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18299004 | deletion | OSC5202 | SNP array | Probe signal intensity | nssv18299003, nssv18299235, nssv18299576 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18299004 | Remapped | Perfect | NC_000004.12:g.(?_ 22713407)_(2277299 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 22,713,407 | 22,772,994 |
| nssv18299004 | Submitted genomic | NC_000004.11:g.(?_ 22715030)_(2277461 7_?)del | GRCh37 (hg19) | NC_000004.11 | Chr4 | 22,715,030 | 22,774,617 |