nsv3965899
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:insertion
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:118,851
- 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: 1253 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 1253 SVs from 81 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 |
---|---|---|---|---|---|---|---|---|---|
nsv3965899 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 157,691,819 | 157,810,669 | ||
nsv3965899 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 157,484,511 | 157,603,361 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15215670 | insertion | Optical mapping | Optical mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15215670 | Submitted genomic | NC_000007.14:g.(15 7691819_?)_(?_1578 10669)ins2509 | GRCh38 (hg38) | NC_000007.14 | Chr7 | 157,691,819 | 157,810,669 | ||
nssv15215670 | Remapped | Perfect | NC_000007.13:g.(15 7484511_?)_(?_1576 03361)ins2509 | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 157,484,511 | 157,603,361 |