nsv1154244
- 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:209
- Description:Insertion of chr11:85347984-85339671
- 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: 410 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 410 SVs from 22 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv1154244 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 122,016,939 | 122,017,147 |
| nsv1154244 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 121,150,792 | 121,151,000 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv4004059 | Remapped | Perfect | NC_000023.11:g.(12 2016939_?)_(?_1220 17147)ins8313 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 122,016,939 | 122,017,147 |
| nssv4004059 | Submitted genomic | NC_000023.10:g.(12 1150792_?)_(?_1211 51000)ins8313 | GRCh37 (hg19) | NC_000023.10 | ChrX | 121,150,792 | 121,151,000 |