nsv7042777
- 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:7,332,033
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: 9718 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 9725 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 |
---|---|---|---|---|---|---|---|---|---|
nsv7042777 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 127,009,007 | 134,341,039 | ||
nsv7042777 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 126,142,990 | 133,475,069 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18765356 | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18765356 | Submitted genomic | NC_000023.11:g.127 009007_134341039in v | GRCh38 (hg38) | NC_000023.11 | ChrX | 127,009,007 | 134,341,039 | ||
nssv18765356 | Remapped | Good | NC_000023.10:g.126 142990_133475069in v | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 126,142,990 | 133,475,069 |
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) |
---|---|---|---|
nssv18765356 | 1.4e-05 | 3 | 214286 |