nsv6573818
- Organism: Homo sapiens
- Study:nstd223 (Sedlazeck et al. 2020)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:7,354,656
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: 19894 SVs from 124 studies. See in: genome view
Overlapping variant regions from other studies: 19896 SVs from 124 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6573818 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 153,431,058 | 160,785,713 | ||
nsv6573818 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 153,752,193 | 161,206,745 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18270036 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18270036 | Submitted genomic | NC_000006.12:g.153 431058_160785713in v | GRCh38 (hg38) | NC_000006.12 | Chr6 | 153,431,058 | 160,785,713 | ||
nssv18270036 | Remapped | Good | NC_000006.11:g.153 752193_161206745in v | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 153,752,193 | 161,206,745 |
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) |
---|---|---|---|
nssv18270036 | 0.288 | 8787 | 30464 |