nsv3114119
- Organism: Homo sapiens
- Study:nstd145 (Lu et al. 2017)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,494
- Publication(s):Lu et al. 2017
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: 304 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 304 SVs from 68 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3114119 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 34,638,639 | 34,645,132 |
| nsv3114119 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 35,104,240 | 35,110,733 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14083976 | Remapped | Perfect | NC_000001.11:g.(?_ 34638639)_(3464513 2_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 34,638,639 | 34,645,132 |
| nssv14095860 | Remapped | Perfect | NC_000001.11:g.(?_ 34638639)_(3464513 2_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 34,638,639 | 34,645,132 |
| nssv14083976 | Submitted genomic | NC_000001.10:g.(?_ 35104240)_(3511073 3_?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 35,104,240 | 35,110,733 | ||
| nssv14095860 | Submitted genomic | NC_000001.10:g.(?_ 35104240)_(3511073 3_?)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 35,104,240 | 35,110,733 |