nsv482984
- Organism: Homo sapiens
- Study:nstd41 (Iafrate et al. 2004)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:179,128
- Publication(s):Iafrate et al. 2004
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: 1069 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 1069 SVs from 86 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv482984 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 133,676,624 | 133,855,751 |
| nsv482984 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 136,541,746 | 136,720,873 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv2996443 | copy number gain | BAC aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv2996443 | Remapped | Perfect | NC_000009.12:g.(?_ 133676624)_(133855 751_?)dup | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 133,676,624 | 133,855,751 |
| nssv2996443 | Submitted genomic | NC_000009.11:g.(?_ 136541746)_(136720 873_?)dup | GRCh37 (hg19) | NC_000009.11 | Chr9 | 136,541,746 | 136,720,873 |