nsv7046288
- 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:12,576
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: 1130 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1130 SVs from 83 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv7046288 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000002.12 | Chr2 | 242,019,646 | 242,032,221 | ||
nsv7046288 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 242,961,797 | 242,974,372 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18769111 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18769111 | Submitted genomic | NC_000002.12:g.242 019646_242032221in v | GRCh38 (hg38) | NC_000002.12 | Chr2 | 242,019,646 | 242,032,221 | ||
nssv18769111 | Remapped | Perfect | NC_000002.11:g.242 961797_242974372in v | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 242,961,797 | 242,974,372 |
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) |
---|---|---|---|
nssv18769111 | <0.001 | 47 | 272022 |