nsv3318134
- Organism: Homo sapiens
- Study:nstd157 (Frenkel et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:13,824
- Publication(s):Frenkel et al. 2019
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: 257 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 257 SVs from 55 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3318134 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 1,924,654 | 1,938,477 |
| nsv3318134 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 1,945,884 | 1,959,707 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14468229 | copy number gain | M2136 | SNP array | SNP genotyping analysis | 54 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14468229 | Remapped | Perfect | NC_000011.10:g.(?_ 1924654)_(1938477_ ?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 1,924,654 | 1,938,477 |
| nssv14468229 | Submitted genomic | NC_000011.9:g.(?_1 945884)_(1959707_? )dup | GRCh37 (hg19) | NC_000011.9 | Chr11 | 1,945,884 | 1,959,707 |