nsv4716262
- 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: 125 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 103 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 129 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 103 SVs from 26 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 |
---|---|---|---|---|---|---|---|---|---|---|
nsv4716262 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 163,012,395 | 163,012,395 | - |
nsv4716262 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 12,256,886 | 12,256,886 | - |
nsv4716262 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 162,982,185 | 162,982,185 | - | ||
nsv4716262 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 12,298,385 | 12,298,385 | - |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
nssv16244522 | interchromosomal translocation | B381 | Sequencing | Paired-end mapping | 1 | 5,743 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
---|---|---|---|---|---|---|---|---|---|
nssv16244522 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 163,012,395 | 163,012,395 | - |
nssv16244522 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 12,256,886 | 12,256,886 | - |
nssv16244522 | Submitted genomic | GRCh37 (hg19) | NC_000001.10 | Chr1 | 162,982,185 | 162,982,185 | - | ||
nssv16244522 | Submitted genomic | GRCh37 (hg19) | NC_000003.11 | Chr3 | 12,298,385 | 12,298,385 | - |