nsv3317568
- 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:23,183
- 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: 581 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 547 SVs from 70 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3317568 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 105,437,914 | 105,461,096 |
| nsv3317568 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 105,904,251 | 105,927,433 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14468236 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv14468236 | Remapped | Perfect | NC_000014.9:g.(?_1 05437914)_(1054610 96_?)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 105,437,914 | 105,461,096 |
| nssv14468236 | Submitted genomic | NC_000014.8:g.(?_1 05904251)_(1059274 33_?)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 105,904,251 | 105,927,433 |