nsv4416027
- 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:449,561
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1303 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 1303 SVs from 80 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4416027 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 83,623,264 | 83,628,120 | 83,963,934 | 84,072,824 |
| nsv4416027 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 84,017,043 | 84,021,899 | 84,357,713 | 84,466,603 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15708973 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15708973 | Remapped | Perfect | NC_000012.12:g.(83 623264_83628120)_( 83963934_84072824) dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 83,623,264 | 83,628,120 | 83,963,934 | 84,072,824 |
| nssv15708973 | Submitted genomic | NC_000012.11:g.(84 017043_84021899)_( 84357713_84466603) dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 84,017,043 | 84,021,899 | 84,357,713 | 84,466,603 |