nsv3965913
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:inversion
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:19,099
- Publication(s):Levy-Sakin 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: 430 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 384 SVs from 63 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3965913 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 1,225,896 | 1,244,994 | ||
nsv3965913 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 1,271,836 | 1,287,046 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15221727 | inversion | Optical mapping | Optical mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15221727 | Submitted genomic | NC_000010.11:g.(12 25896_?)_(?_124499 4)inv | GRCh38 (hg38) | NC_000010.11 | Chr10 | 1,225,896 | 1,244,994 | ||
nssv15221727 | Remapped | Pass | NC_000010.10:g.(12 71836_?)_(?_128704 6)inv | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 1,271,836 | 1,287,046 |