nsv6633542
- 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:240,596
- 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: 774 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 777 SVs from 79 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6633542 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 71,076,267 | 71,316,862 |
| nsv6633542 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 73,691,183 | 73,931,778 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18299945 | duplication | OSC5256 | SNP array | Probe signal intensity | nssv18299946, nssv18299948 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18299945 | Remapped | Perfect | NC_000009.12:g.(?_ 71076267)_(7131686 2_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 71,076,267 | 71,316,862 |
| nssv18299945 | Submitted genomic | NC_000009.11:g.(?_ 73691183)_(7393177 8_?)dup | GRCh37 (hg19) | NC_000009.11 | Chr9 | 73,691,183 | 73,931,778 |