nsv3247289
- Organism: Homo sapiens
- Study:nstd152 (Chaisson et al. 2019)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:22,206
- Publication(s):Chaisson et al. 2019
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: 233 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 233 SVs from 49 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3247289 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 99,761,521 (-15, +15) | 99,783,726 (-15, +15) | ||
nsv3247289 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 99,632,252 (-15, +15) | 99,654,457 (-15, +15) |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14360931 | Submitted genomic | NC_000011.10:g.(99 761506_99761536)_( 99783711_99783741) inv22205 | GRCh38 (hg38) | NC_000011.10 | Chr11 | 99,761,521 (-15, +15) | 99,783,726 (-15, +15) | ||
nssv14360932 | Submitted genomic | NC_000011.10:g.(99 761506_99761536)_( 99783711_99783741) inv22205 | GRCh38 (hg38) | NC_000011.10 | Chr11 | 99,761,521 (-15, +15) | 99,783,726 (-15, +15) | ||
nssv14360931 | Remapped | Perfect | NC_000011.9:g.(996 32237_99632267)_(9 9654442_99654472)i nv22205 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 99,632,252 (-15, +15) | 99,654,457 (-15, +15) |
nssv14360932 | Remapped | Perfect | NC_000011.9:g.(996 32237_99632267)_(9 9654442_99654472)i nv22205 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 99,632,252 (-15, +15) | 99,654,457 (-15, +15) |