nsv3071807
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Data Source:HUMANGENOME_JCVI
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: 237 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 237 SVs from 30 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3071807 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 99,430,373 | 99,430,373 |
| nsv3071807 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 100,082,627 | 100,082,627 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14041885 | insertion | 1104685250318 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14041885 | Remapped | Perfect | NC_000013.11:g.994 30373_99430374ins2 55 | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 99,430,373 | 99,430,373 |
| nssv14041885 | Submitted genomic | NC_000013.10:g.100 082627_100082628in s255 | GRCh37 (hg19) | NC_000013.10 | Chr13 | 100,082,627 | 100,082,627 |