nsv3071836
- 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: 88 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 88 SVs from 26 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3071836 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 96,415,762 | 96,415,762 |
| nsv3071836 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 98,175,519 | 98,175,519 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14041339 | insertion | 1104685168250 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14041339 | Remapped | Perfect | NC_000010.11:g.964 15762_96415763ins2 55 | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 96,415,762 | 96,415,762 |
| nssv14041339 | Submitted genomic | NC_000010.10:g.981 75519_98175520ins2 55 | GRCh37 (hg19) | NC_000010.10 | Chr10 | 98,175,519 | 98,175,519 |