nsv932796
- Organism: Homo sapiens
- Study:nstd79 (Dittwald et al. 2013)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,215,082
- Publication(s):Dittwald et al. 2013
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: 7421 SVs from 115 studies. See in: genome view
Overlapping variant regions from other studies: 7422 SVs from 115 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv932796 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 72,607,830 | 72,607,830 | 75,822,911 | 75,822,911 |
| nsv932796 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 72,900,171 | 72,963,539 | 75,973,121 | 76,115,252 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv1611205 | deletion | 1794 | Oligo aCGH | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv1611205 | Remapped | Perfect | NC_000015.10:g.(72 685862_72685862)_( 75339830_75339830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 72,685,862 | 72,685,862 | 75,339,830 | 75,339,830 |
| nssv1611205 | Submitted genomic | NC_000015.9:g.(729 78203_72978374)_(7 5631888_75632171)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 72,978,203 | 72,978,374 | 75,631,888 | 75,632,171 |