nsv984648
- Organism: Homo sapiens
- Study:nstd92 (Forsberg et al. 2014)
- Variant Type:complex substitution
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:82,404,196
- 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: 237597 SVs from 151 studies. See in: genome view
Overlapping variant regions from other studies: 235287 SVs from 151 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv984648 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 24,475,261 | 106,879,456 |
| nsv984648 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 24,944,467 | 107,287,663 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv3217266 | complex substitution | ULSAM546 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3217266 | Remapped | Good | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 24,475,261 | 106,879,456 |
| nssv3217266 | Submitted genomic | GRCh37 (hg19) | NC_000014.8 | Chr14 | 24,944,467 | 107,287,663 |