nsv6632090
- 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:28,628
- 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: 634 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 447 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 458 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 683 SVs from 83 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6632090 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 43,748 | 72,375 |
| nsv6632090 | Remapped | Good | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187558.1 | Chr7|NT_18 7558.1 | 1 | 28,474 |
| nsv6632090 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_2 | Second Pass | NT_187653.1 | Chr7|NT_18 7653.1 | 36,069 | 64,696 |
| nsv6632090 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 43,748 | 72,375 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18315246 | deletion | OSC7990 | SNP array | Probe signal intensity | 9 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18315246 | Remapped | Good | NT_187558.1:g.(?_1 )_(28474_?)del | GRCh38.p12 | Second Pass | NT_187558.1 | Chr7|NT_18 7558.1 | 1 | 28,474 |
| nssv18315246 | Remapped | Perfect | NT_187653.1:g.(?_3 6069)_(64696_?)del | GRCh38.p12 | Second Pass | NT_187653.1 | Chr7|NT_18 7653.1 | 36,069 | 64,696 |
| nssv18315246 | Remapped | Perfect | NC_000007.14:g.(?_ 43748)_(72375_?)de l | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 43,748 | 72,375 |
| nssv18315246 | Submitted genomic | NC_000007.13:g.(?_ 43748)_(72375_?)de l | GRCh37 (hg19) | NC_000007.13 | Chr7 | 43,748 | 72,375 |