nsv4420280
- Organism: Homo sapiens
- Study:nstd174 (DGV Gold Standard)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:409,864
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1763 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 1763 SVs from 85 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4420280 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 66,316,916 | 66,316,916 | 66,722,766 | 66,726,779 |
| nsv4420280 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000018.9 | Chr18 | 63,984,153 | 63,984,153 | 64,390,003 | 64,394,016 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15710058 | copy number gain | Multiple | Multiple |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15710058 | Remapped | Perfect | NC_000018.10:g.(66 316916_66316916)_( 66722766_66726779) dup | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 66,316,916 | 66,316,916 | 66,722,766 | 66,726,779 |
| nssv15710058 | Submitted genomic | NC_000018.9:g.(639 84153_63984153)_(6 4390003_64394016)d up | GRCh37 (hg19) | NC_000018.9 | Chr18 | 63,984,153 | 63,984,153 | 64,390,003 | 64,394,016 |