nsv1154179
- Organism: Homo sapiens
- Study:nstd105 (Onozawa et al. 2015)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:389
- Description:Insertion of chr12:112734994-112734944
- Publication(s):Onozawa et al. 2015
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: 132 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154179 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 71,356,025 | 71,356,413 |
| nsv1154179 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 72,221,742 | 72,222,130 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv4004064 | insertion | NA18555 | Sequencing | Sequence alignment | nssv4004072, nssv4004139 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004064 | Remapped | Perfect | NC_000004.12:g.(71 356025_?)_(?_71356 413)ins50 | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 71,356,025 | 71,356,413 |
| nssv4004064 | Submitted genomic | NC_000004.11:g.(72 221742_?)_(?_72222 130)ins50 | GRCh37 (hg19) | NC_000004.11 | Chr4 | 72,221,742 | 72,222,130 |