nsv4429011
- 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:410,915
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1318 SVs from 78 studies. See in: genome view
Overlapping variant regions from other studies: 1440 SVs from 78 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4429011 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 46,429,858 | 46,432,081 | 46,740,415 | 46,840,772 |
| nsv4429011 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 46,463,770 | 46,465,993 | 46,774,327 | 46,874,684 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15709645 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15709645 | Remapped | Perfect | NC_000016.10:g.(46 429858_46432081)_( 46740415_46840772) dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 46,429,858 | 46,432,081 | 46,740,415 | 46,840,772 |
| nssv15709645 | Submitted genomic | NC_000016.9:g.(464 63770_46465993)_(4 6774327_46874684)d up | GRCh37 (hg19) | NC_000016.9 | Chr16 | 46,463,770 | 46,465,993 | 46,774,327 | 46,874,684 |