nsv6624180
- 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:102,804
- 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: 733 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 733 SVs from 65 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6624180 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 8,708,895 | 8,811,698 |
| nsv6624180 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 8,802,752 | 8,905,555 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18313732 | duplication | OSC0823 | SNP array | Probe signal intensity | nssv18314416, nssv18314175, nssv18314407 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18313732 | Remapped | Perfect | NC_000016.10:g.(?_ 8708895)_(8811698_ ?)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 8,708,895 | 8,811,698 |
| nssv18313732 | Submitted genomic | NC_000016.9:g.(?_8 802752)_(8905555_? )dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 8,802,752 | 8,905,555 |