nsv1154291
- 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:313
- Description:Insertion of chr5:112203524-112203604
- 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: 127 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 127 SVs from 24 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 |
---|---|---|---|---|---|---|---|---|---|
nsv1154291 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 40,629,472 | 40,629,784 |
nsv1154291 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000019.9 | Chr19 | 41,135,377 | 41,135,689 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv4004132 | insertion | NA18526 | Sequencing | Sequence alignment | nssv4004056, nssv4004124, nssv4004194 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv4004132 | Remapped | Perfect | NC_000019.10:g.(40 629472_?)_(?_40629 784)ins80 | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 40,629,472 | 40,629,784 |
nssv4004132 | Submitted genomic | NC_000019.9:g.(411 35377_?)_(?_411356 89)ins80 | GRCh37 (hg19) | NC_000019.9 | Chr19 | 41,135,377 | 41,135,689 |