nsv3110436
- Organism: Homo sapiens
- Study:nstd145 (Lu et al. 2017)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:170,915
- Publication(s):Lu et al. 2017
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: 1057 SVs from 87 studies. See in: genome view
Overlapping variant regions from other studies: 1057 SVs from 87 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3110436 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 65,843,447 | 66,014,361 |
| nsv3110436 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 63,510,683 | 63,681,597 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14100267 | duplication | sample364 | Oligo aCGH | Probe signal intensity | 95 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14100267 | Remapped | Perfect | NC_000018.10:g.(?_ 65843447)_(6601436 1_?)dup | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 65,843,447 | 66,014,361 |
| nssv14100267 | Submitted genomic | NC_000018.9:g.(?_6 3510683)_(63681597 _?)dup | GRCh37 (hg19) | NC_000018.9 | Chr18 | 63,510,683 | 63,681,597 |