nsv4360652
- Organism: Homo sapiens
- Study:nstd169 (Giner-Delgado et al. 2019)
- Variant Type:inversion
- Method Type:MLPA
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,663
- Publication(s):Giner-Delgado 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: 133 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 133 SVs from 42 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4360652 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 41,320,652 | 41,320,670 | 41,321,621 | 41,322,314 |
nsv4360652 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000003.11 | Chr3 | 41,362,143 | 41,362,161 | 41,363,112 | 41,363,805 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15607174 | inversion | MLPA | Genotyping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15607174 | Remapped | Perfect | NC_000003.12:g.(41 320652_41320670)_( 41321621_41322314) inv | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 41,320,652 | 41,320,670 | 41,321,621 | 41,322,314 |
nssv15607174 | Submitted genomic | NC_000003.11:g.(41 362143_41362161)_( 41363112_41363805) inv | GRCh37.p13 | NC_000003.11 | Chr3 | 41,362,143 | 41,362,161 | 41,363,112 | 41,363,805 |