nsv3071802
- 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: 165 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3071802 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 225,964,566 | 225,964,566 |
| nsv3071802 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 226,152,266 | 226,152,266 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14041881 | insertion | 1104685057618 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14041881 | Remapped | Perfect | NC_000001.11:g.225 964566_225964567in s186 | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 225,964,566 | 225,964,566 |
| nssv14041881 | Submitted genomic | NC_000001.10:g.226 152266_226152267in s186 | GRCh37 (hg19) | NC_000001.10 | Chr1 | 226,152,266 | 226,152,266 |