nsv2754894
- 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:16,360
- 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: 111 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 111 SVs from 31 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv2754894 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 62,803,942 | 62,820,301 |
| nsv2754894 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 64,563,702 | 64,580,061 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv13624426 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv13624426 | Remapped | Perfect | NC_000010.11:g.(?_ 62803942)_(6282030 1_?)del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 62,803,942 | 62,820,301 |
| nssv13624426 | Submitted genomic | NC_000010.10:g.(?_ 64563702)_(6458006 1_?)del | GRCh37 (hg19) | NC_000010.10 | Chr10 | 64,563,702 | 64,580,061 |