nsv984624
- Organism: Homo sapiens
- Study:nstd92 (Forsberg et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,939,415
- Publication(s):Forsberg et al. 2014
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: 7760 SVs from 117 studies. See in: genome view
Overlapping variant regions from other studies: 7729 SVs from 117 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv984624 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 85,333,874 | 88,273,288 |
| nsv984624 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 85,044,918 | 88,006,456 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv3217333 | copy number gain | ULSAM1581 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3217333 | Remapped | Good | NC_000011.10:g.(?_ 85333874)_(8827328 8_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 85,333,874 | 88,273,288 |
| nssv3217333 | Submitted genomic | NC_000011.9:g.(?_8 5044918)_(88006456 _?)dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 85,044,918 | 88,006,456 |