nsv2760796
- Organism: Homo sapiens
- Study:nstd130 (Leppa et al. 2016)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,325,051
- Publication(s):Leppa et al. 2016
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: 5461 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 4424 SVs from 94 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv2760796 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 34,679,969 | 38,005,019 |
| nsv2760796 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 34,832,904 | 38,398,821 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv13625927 | deletion | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv13625927 | Remapped | Pass | NC_000012.12:g.(?_ 34679969)_(3800501 9_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 34,679,969 | 38,005,019 |
| nssv13625927 | Submitted genomic | NC_000012.11:g.(?_ 34832904)_(3839882 1_?)del | GRCh37 (hg19) | NC_000012.11 | Chr12 | 34,832,904 | 38,398,821 |