nsv4375827
- Organism: Homo sapiens
- Study:nstd173 (Zarrei 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:145,116
- Publication(s):Zarrei 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: 1953 SVs from 88 studies. See in: genome view
Overlapping variant regions from other studies: 1953 SVs from 88 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4375827 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 832,628 | 977,743 |
| nsv4375827 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 735,868 | 880,983 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15683518 | Remapped | Perfect | NC_000017.11:g.(?_ 832628)_(977743_?) dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 832,628 | 977,743 |
| nssv15689095 | Remapped | Perfect | NC_000017.11:g.(?_ 832628)_(977743_?) dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 832,628 | 977,743 |
| nssv15683518 | Submitted genomic | NC_000017.10:g.(?_ 735868)_(880983_?) dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 735,868 | 880,983 | ||
| nssv15689095 | Submitted genomic | NC_000017.10:g.(?_ 735868)_(880983_?) dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 735,868 | 880,983 |