nsv3418829
- Organism: Homo sapiens
- Study:nstd164 (Karolak et al. 2019)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:10,449
- Publication(s):Karolak et al. 2019
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: 188 SVs from 33 studies. See in: genome view
Overlapping variant regions from other studies: 188 SVs from 33 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv3418829 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 60,780,528 | 60,780,537 | 60,790,967 | 60,790,976 |
| nsv3418829 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 58,857,889 | 58,857,898 | 58,868,328 | 58,868,337 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14814885 | copy number loss | P038 | Oligo aCGH | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv14814885 | Remapped | Perfect | NC_000017.11:g.(60 780528_60780537)_( 60790967_60790976) del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 60,780,528 | 60,780,537 | 60,790,967 | 60,790,976 |
| nssv14814885 | Submitted genomic | NC_000017.10:g.(58 857889_58857898)_( 58868328_58868337) del | GRCh37 (hg19) | NC_000017.10 | Chr17 | 58,857,889 | 58,857,898 | 58,868,328 | 58,868,337 |