nsv4360635
- 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:18,962
- 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: 197 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 196 SVs from 46 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv4360635 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 71,564,791 | 71,571,819 | 71,576,725 | 71,583,752 |
| nsv4360635 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000011.9 | Chr11 | 71,275,837 | 71,282,865 | 71,287,771 | 71,294,798 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15607145 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv15607145 | Remapped | Perfect | NC_000011.10:g.(71 564791_71571819)_( 71576725_71583752) inv | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 71,564,791 | 71,571,819 | 71,576,725 | 71,583,752 |
| nssv15607145 | Submitted genomic | NC_000011.9:g.(712 75837_71282865)_(7 1287771_71294798)i nv | GRCh37.p13 | NC_000011.9 | Chr11 | 71,275,837 | 71,282,865 | 71,287,771 | 71,294,798 |