nsv6112625
- Organism: Homo sapiens
- Study:nstd212 (Wu 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):Wu 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: 128 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 128 SVs from 25 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6112625 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000020.11 | Chr20 | 44,061,937 | 44,061,937 | ||
nsv6112625 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 42,690,577 | 42,690,577 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17617960 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17617960 | Submitted genomic | NC_000020.11:g.440 61937_44061938ins3 13 | GRCh38 (hg38) | NC_000020.11 | Chr20 | 44,061,937 | 44,061,937 | ||
nssv17617960 | Remapped | Perfect | NC_000020.10:g.426 90577_42690578ins3 13 | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 42,690,577 | 42,690,577 |