nsv4360640
- 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:32,391
- 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: 234 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 234 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv4360640 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 141,866,324 | 141,866,325 | 141,898,713 | 141,898,714 |
nsv4360640 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000006.11 | Chr6 | 142,187,461 | 142,187,462 | 142,219,850 | 142,219,851 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15607178 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv15607178 | Remapped | Perfect | NC_000006.12:g.(14 1866324_141866325) _(141898713_141898 714)inv | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 141,866,324 | 141,866,325 | 141,898,713 | 141,898,714 |
nssv15607178 | Submitted genomic | NC_000006.11:g.(14 2187461_142187462) _(142219850_142219 851)inv | GRCh37.p13 | NC_000006.11 | Chr6 | 142,187,461 | 142,187,462 | 142,219,850 | 142,219,851 |