nsv4418088
- 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:51
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 123 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 120 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4418088 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 57,745,345 | 57,745,345 | 57,745,395 | 57,745,395 |
| nsv4418088 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 57,779,257 | 57,779,257 | 57,779,307 | 57,779,307 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15723965 | copy number loss | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15723965 | Remapped | Perfect | NC_000016.10:g.(57 745345_57745345)_( 57745395_57745395) del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 57,745,345 | 57,745,345 | 57,745,395 | 57,745,395 |
| nssv15723965 | Submitted genomic | NC_000016.9:g.(577 79257_57779257)_(5 7779307_57779307)d el | GRCh37 (hg19) | NC_000016.9 | Chr16 | 57,779,257 | 57,779,257 | 57,779,307 | 57,779,307 |