nsv5345806
- Organism: Homo sapiens
- Study:nstd200 (Abel et al. 2020)
- Variant Type:translocation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Abel et al. 2020
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 24 studies. See in: genome view
Overlapping variant regions from other studies: 229 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 199 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 229 SVs from 35 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv5345806 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 52,167,391 | 52,167,391 | + |
| nsv5345806 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 52,376,794 | 52,376,794 | + |
| nsv5345806 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 52,741,526 | 52,741,526 | + | ||
| nsv5345806 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 52,950,929 | 52,950,929 | + |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16397842 | intrachromosomal translocation | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv16397842 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 52,167,391 | 52,167,391 | + |
| nssv16397842 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 52,376,794 | 52,376,794 | + |
| nssv16397842 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 52,741,526 | 52,741,526 | + | ||
| nssv16397842 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 52,950,929 | 52,950,929 | + |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16397842 | <0.001 | 6 | 16834 |