nsv984821
- 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:69,781,861
- 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: 183378 SVs from 144 studies. See in: genome view
Overlapping variant regions from other studies: 183171 SVs from 144 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv984821 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 75,294,181 | 145,076,041 |
| nsv984821 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 76,206,416 | 146,301,427 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3217236 | copy number gain | ULSAM298 | SNP array | SNP genotyping analysis | nssv3217239, nssv3217235, nssv3217233 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3217236 | Remapped | Good | NC_000008.11:g.(?_ 75294181)_(1450760 41_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 75,294,181 | 145,076,041 |
| nssv3217236 | Submitted genomic | NC_000008.10:g.(?_ 76206416)_(1463014 27_?)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 76,206,416 | 146,301,427 |