nsv5663666
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Ebert et al. 2021
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: 327 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 327 SVs from 47 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5663666 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 84,479,390 | 84,479,390 | ||
nsv5663666 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 84,512,996 | 84,512,996 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv17088597 | insertion | HG03065 | Sequencing | Sequence alignment | 3,836 |
nssv17093141 | insertion | SAMN00001694 | Sequencing | Sequence alignment | 8,610 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17088597 | Submitted genomic | NC_000016.10:g.844 79390_84479391ins1 34 | GRCh38 (hg38) | NC_000016.10 | Chr16 | 84,479,390 | 84,479,390 | ||
nssv17093141 | Submitted genomic | NC_000016.10:g.844 79390_84479391ins5 8 | GRCh38 (hg38) | NC_000016.10 | Chr16 | 84,479,390 | 84,479,390 | ||
nssv17088597 | Remapped | Perfect | NC_000016.9:g.8451 2996_84512997ins13 4 | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 84,512,996 | 84,512,996 |
nssv17093141 | Remapped | Perfect | NC_000016.9:g.8451 2996_84512997ins58 | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 84,512,996 | 84,512,996 |