nsv3318155
- Organism: Homo sapiens
- Study:nstd157 (Frenkel et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:163,902
- Publication(s):Frenkel 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: 965 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 965 SVs from 73 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3318155 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 4,773,037 | 4,936,938 |
| nsv3318155 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000019.9 | Chr19 | 4,773,049 | 4,936,950 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14471481 | Remapped | Perfect | NC_000019.10:g.(?_ 4773037)_(4936938_ ?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 4,773,037 | 4,936,938 |
| nssv14471546 | Remapped | Perfect | NC_000019.10:g.(?_ 4773037)_(4936938_ ?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 4,773,037 | 4,936,938 |
| nssv14471481 | Submitted genomic | NC_000019.9:g.(?_4 773049)_(4936950_? )del | GRCh37 (hg19) | NC_000019.9 | Chr19 | 4,773,049 | 4,936,950 | ||
| nssv14471546 | Submitted genomic | NC_000019.9:g.(?_4 773049)_(4936950_? )del | GRCh37 (hg19) | NC_000019.9 | Chr19 | 4,773,049 | 4,936,950 |