nsv4715834
- 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: 199 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 106 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 199 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 106 SVs from 25 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 |
---|---|---|---|---|---|---|---|---|---|---|
nsv4715834 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 132,342,373 | 132,342,373 | + |
nsv4715834 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 44,362,016 | 44,362,016 | + |
nsv4715834 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 133,099,946 | 133,099,946 | + | ||
nsv4715834 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000019.9 | Chr19 | 44,866,174 | 44,866,174 | + |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
nssv16238444 | interchromosomal translocation | M478 | Sequencing | Paired-end mapping | 1 | 4,557 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
---|---|---|---|---|---|---|---|---|---|
nssv16238444 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 132,342,373 | 132,342,373 | + |
nssv16238444 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 44,362,016 | 44,362,016 | + |
nssv16238444 | Submitted genomic | GRCh37 (hg19) | NC_000002.11 | Chr2 | 133,099,946 | 133,099,946 | + | ||
nssv16238444 | Submitted genomic | GRCh37 (hg19) | NC_000019.9 | Chr19 | 44,866,174 | 44,866,174 | + |