nsv3166895
- Organism: Homo sapiens
- Study:nstd151 (Exome Aggregation Consortium CNVs)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:314
- Description:qual score = 78
- Publication(s):Exome Aggregation Consortium CNVs
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: 142 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 140 SVs from 23 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3166895 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 42,979,375 | 42,979,688 |
| nsv3166895 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 41,131,392 | 41,131,705 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv14211325 | copy number gain | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14211325 | Remapped | Perfect | NC_000017.11:g.(?_ 42979375)_(4297968 8_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 42,979,375 | 42,979,688 |
| nssv14211325 | Submitted genomic | NC_000017.10:g.(?_ 41131392)_(4113170 5_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 41,131,392 | 41,131,705 |