nsv7057713
- Organism: Homo sapiens
- Study:nstd229 (Jun et al. 2023)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,169,795
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: 3033 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 3471 SVs from 97 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv7057713 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 56,332,234 | 57,502,028 | ||
nsv7057713 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 56,197,032 | 57,366,927 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18779841 | inversion | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18779841 | Submitted genomic | NC_000006.12:g.563 32234_57502028inv | GRCh38 (hg38) | NC_000006.12 | Chr6 | 56,332,234 | 57,502,028 | ||
nssv18779841 | Remapped | Good | NC_000006.11:g.561 97032_57366927inv | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 56,197,032 | 57,366,927 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
---|---|---|---|
nssv18779841 | 7e-06 | 2 | 276268 |