nsv4369096
- Organism: Homo sapiens
- Study:nstd173 (Zarrei 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:472,544
- Publication(s):Zarrei 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: 1344 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 1341 SVs from 95 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4369096 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 110,167,679 | 110,640,222 |
| nsv4369096 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 110,925,256 | 111,397,799 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15667641 | copy number gain | 5-1000-003 | SNP array | Genotyping | 18 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15667641 | Remapped | Perfect | NC_000002.12:g.(?_ 110167679)_(110640 222_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 110,167,679 | 110,640,222 |
| nssv15667641 | Submitted genomic | NC_000002.11:g.(?_ 110925256)_(111397 799_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 110,925,256 | 111,397,799 |