nsv5662223
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- 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: 285 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 285 SVs from 29 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5662223 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000018.10 | Chr18 | 12,491,252 | 12,491,252 | ||
nsv5662223 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 12,491,251 | 12,491,251 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17100159 | Submitted genomic | NC_000018.10:g.124 91252_12491253ins6 228 | GRCh38 (hg38) | NC_000018.10 | Chr18 | 12,491,252 | 12,491,252 | ||
nssv17100159 | Remapped | Perfect | NC_000018.9:g.1249 1251_12491252ins62 28 | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 12,491,251 | 12,491,251 |