nsv6631553
- 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:74,573
- 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: 745 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 745 SVs from 74 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6631553 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 94,680,468 | 94,755,040 |
| nsv6631553 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 95,390,186 | 95,464,758 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18296074 | deletion | OSC4686 | SNP array | Probe signal intensity | nssv18297340, nssv18297342, nssv18296450 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18296074 | Remapped | Perfect | NC_000006.12:g.(?_ 94680468)_(9475504 0_?)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 94,680,468 | 94,755,040 |
| nssv18296074 | Submitted genomic | NC_000006.11:g.(?_ 95390186)_(9546475 8_?)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 95,390,186 | 95,464,758 |