nsv6633326
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:64,505
- 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: 2205 SVs from 82 studies. See in: genome view
Overlapping variant regions from other studies: 2209 SVs from 82 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6633326 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 11,949,207 | 12,013,711 |
| nsv6633326 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 11,949,207 | 12,013,711 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18301984 | deletion | OSC5623 | SNP array | Probe signal intensity | nssv18300707, nssv18300708, nssv18300709 |
| nssv18321395 | deletion | OSC1098 | SNP array | Probe signal intensity | 6 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18301984 | Remapped | Perfect | NC_000009.12:g.(?_ 11949207)_(1201371 1_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 11,949,207 | 12,013,711 |
| nssv18321395 | Remapped | Perfect | NC_000009.12:g.(?_ 11949207)_(1201371 1_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 11,949,207 | 12,013,711 |
| nssv18301984 | Submitted genomic | NC_000009.11:g.(?_ 11949207)_(1201371 1_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 11,949,207 | 12,013,711 | ||
| nssv18321395 | Submitted genomic | NC_000009.11:g.(?_ 11949207)_(1201371 1_?)del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 11,949,207 | 12,013,711 |