nsv4716260
- Organism: Homo sapiens
- Study:nstd195 (Mwapagha et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2
- Publication(s):Mwapagha et al. 2021
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: 114 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 114 SVs from 32 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4716260 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 10,685,912 | 10,685,913 |
nsv4716260 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 10,826,038 | 10,826,039 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
nssv16248818 | inversion | B450 | Sequencing | Paired-end mapping | 1 | 4,473 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16248818 | Remapped | Perfect | NC_000002.12:g.106 85912_10685913inv | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 10,685,912 | 10,685,913 |
nssv16248818 | Submitted genomic | NC_000002.11:g.108 26038_10826039inv | GRCh37 (hg19) | NC_000002.11 | Chr2 | 10,826,038 | 10,826,039 |