nsv5976825
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Almarri et al. 2020
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: 134 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 134 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 |
---|---|---|---|---|---|---|---|---|---|
nsv5976825 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 31,060,262 | 31,060,262 | ||
nsv5976825 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 31,081,809 | 31,081,809 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17366095 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17366095 | Submitted genomic | NC_000011.10:g.310 60262_31060263ins1 30 | GRCh38 (hg38) | NC_000011.10 | Chr11 | 31,060,262 | 31,060,262 | ||
nssv17366095 | Remapped | Perfect | NC_000011.9:g.3108 1809_31081810ins13 0 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 31,081,809 | 31,081,809 |