nsv5338235
- 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: 82 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 259 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 82 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 259 SVs from 38 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv5338235 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 110,475,039 | 110,475,039 | - |
| nsv5338235 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 21,154,052 | 21,154,052 | - |
| nsv5338235 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 110,912,844 | 110,912,844 | - | ||
| nsv5338235 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 21,728,191 | 21,728,191 | - |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16401508 | interchromosomal translocation | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv16401508 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 110,475,039 | 110,475,039 | - |
| nssv16401508 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 21,154,052 | 21,154,052 | - |
| nssv16401508 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 110,912,844 | 110,912,844 | - | ||
| nssv16401508 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 21,728,191 | 21,728,191 | - |
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) |
|---|---|---|---|
| nssv16401508 | <0.001 | 1 | 16834 |