nsv893369
- Organism: Homo sapiens
- Study:nstd71 (Xu et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:488,921
- Publication(s):Xu et al. 2011
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: 2042 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 1017 SVs from 24 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv893369 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 66,605,578 | 66,605,578 | 67,094,498 | 67,094,498 |
| nsv893369 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 66,345,398 | 66,541,522 | 66,824,235 | 66,834,318 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1519854 | copy number gain | SP50580 | SNP array | SNP genotyping analysis | 13 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv1519854 | Remapped | Perfect | NC_000009.11:g.(66 605578_66605578)_( 67094498_67094498) dup | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 66,605,578 | 66,605,578 | 67,094,498 | 67,094,498 |
| nssv1519854 | Submitted genomic | NC_000009.10:g.(66 345398_66541522)_( 66824235_66834318) dup | NCBI36 (hg18) | NC_000009.10 | Chr9 | 66,345,398 | 66,541,522 | 66,824,235 | 66,834,318 |