nsv1154271
- 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:331
- Description:Insertion of chr22:50354470-50357719
- 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: 246 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 246 SVs from 26 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 |
---|---|---|---|---|---|---|---|---|---|
nsv1154271 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 1,575,959 | 1,576,289 |
nsv1154271 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 1,625,960 | 1,626,290 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis |
---|---|---|---|---|
nssv4004113 | insertion | NA19704 | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv4004113 | Remapped | Perfect | NC_000016.10:g.(15 75959_?)_(?_157628 9)ins3249 | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 1,575,959 | 1,576,289 |
nssv4004113 | Submitted genomic | NC_000016.9:g.(162 5960_?)_(?_1626290 )ins3249 | GRCh37 (hg19) | NC_000016.9 | Chr16 | 1,625,960 | 1,626,290 |