nsv4711063
- Organism: Homo sapiens
- Study:nstd195 (Mwapagha et al. 2021)
- Variant Type:translocation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- 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: 92 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 1697 SVs from 80 studies. See in: genome view
Overlapping variant regions from other studies: 86 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 1699 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 | Start | Stop | strand |
---|---|---|---|---|---|---|---|---|---|---|
nsv4711063 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 42,834,670 | 42,834,670 | - |
nsv4711063 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 33,683,487 | 33,683,487 | - |
nsv4711063 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 43,330,118 | 43,330,118 | - | ||
nsv4711063 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 33,485,954 | 33,485,954 | - |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
nssv16247007 | interchromosomal translocation | B450 | Sequencing | Paired-end mapping | 1 | 4,473 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
---|---|---|---|---|---|---|---|---|---|
nssv16247007 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 42,834,670 | 42,834,670 | - |
nssv16247007 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 33,683,487 | 33,683,487 | - |
nssv16247007 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 43,330,118 | 43,330,118 | - | ||
nssv16247007 | Submitted genomic | GRCh37 (hg19) | NC_000016.9 | Chr16 | 33,485,954 | 33,485,954 | - |