nsv3067541
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:delins
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,192
- 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: 321 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 321 SVs from 52 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3067541 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 198,003,886 | 198,005,077 |
| nsv3067541 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 197,730,757 | 197,731,948 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14039023 | delins | 1104685048961 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14039023 | Remapped | Perfect | NC_000003.12:g.198 003886_198005077de lins776 | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 198,003,886 | 198,005,077 |
| nssv14039023 | Submitted genomic | NC_000003.11:g.197 730757_197731948de lins776 | GRCh37 (hg19) | NC_000003.11 | Chr3 | 197,730,757 | 197,731,948 |