nsv3115560
- 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:3,555
- 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: 210 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 210 SVs from 38 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv3115560 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 96,249,002 | 96,252,556 |
| nsv3115560 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 97,261,230 | 97,264,784 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14087018 | Remapped | Perfect | NC_000008.11:g.(?_ 96249002)_(9625255 6_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 96,249,002 | 96,252,556 |
| nssv14088329 | Remapped | Perfect | NC_000008.11:g.(?_ 96249002)_(9625255 6_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 96,249,002 | 96,252,556 |
| nssv14087018 | Submitted genomic | NC_000008.10:g.(?_ 97261230)_(9726478 4_?)del | GRCh37 (hg19) | NC_000008.10 | Chr8 | 97,261,230 | 97,264,784 | ||
| nssv14088329 | Submitted genomic | NC_000008.10:g.(?_ 97261230)_(9726478 4_?)del | GRCh37 (hg19) | NC_000008.10 | Chr8 | 97,261,230 | 97,264,784 |