nsv7074060
- 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:159,147
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: 641 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 641 SVs from 71 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv7074060 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 51,672,076 | 51,831,222 | ||
nsv7074060 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 52,584,636 | 52,743,782 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18782488 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18782488 | Submitted genomic | NC_000008.11:g.516 72076_51831222inv | GRCh38 (hg38) | NC_000008.11 | Chr8 | 51,672,076 | 51,831,222 | ||
nssv18782488 | Remapped | Perfect | NC_000008.10:g.525 84636_52743782inv | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 52,584,636 | 52,743,782 |
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) |
---|---|---|---|
nssv18782488 | <0.001 | 43 | 269846 |