nsv1154167
- 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:387
- Description:Insertion of chr6:24810722-24810767
- 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: 92 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 92 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154167 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 71,203,152 | 71,203,538 |
| nsv1154167 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 71,430,282 | 71,430,668 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv4004139 | insertion | NA18555 | Sequencing | Sequence alignment | nssv4004064, nssv4004072 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004139 | Remapped | Perfect | NC_000002.12:g.(71 203152_?)_(?_71203 538)ins45 | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 71,203,152 | 71,203,538 |
| nssv4004139 | Submitted genomic | NC_000002.11:g.(71 430282_?)_(?_71430 668)ins45 | GRCh37 (hg19) | NC_000002.11 | Chr2 | 71,430,282 | 71,430,668 |