nsv6131991
- Organism: Homo sapiens
- Study:nstd213 (Pham et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:45,810
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: 392 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 392 SVs from 75 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv6131991 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 1,894,025 | 1,894,042 | 1,939,805 | 1,939,834 |
nsv6131991 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 1,915,255 | 1,915,272 | 1,961,035 | 1,961,064 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv17682414 | inversion | SAMN20524665 | Sequencing | Paired-end mapping | 405 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv17682414 | Remapped | Perfect | NC_000011.10:g.(18 94025_1894042)_(19 39805_1939834)inv | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 1,894,025 | 1,894,042 | 1,939,805 | 1,939,834 |
nssv17682414 | Submitted genomic | NC_000011.9:g.(191 5255_1915272)_(196 1035_1961064)inv | GRCh37 (hg19) | NC_000011.9 | Chr11 | 1,915,255 | 1,915,272 | 1,961,035 | 1,961,064 |