nsv5662260
- 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: 321 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 324 SVs from 34 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5662260 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000013.11 | Chr13 | 113,541,858 | 113,541,858 | ||
nsv5662260 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 114,196,173 | 114,196,173 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17089620 | Submitted genomic | NC_000013.11:g.113 541858_113541859in s2265 | GRCh38 (hg38) | NC_000013.11 | Chr13 | 113,541,858 | 113,541,858 | ||
nssv17089620 | Remapped | Perfect | NC_000013.10:g.114 196173_114196174in s2265 | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 114,196,173 | 114,196,173 |