nsv6907486
- Organism: Homo sapiens
- Study:nstd229 (Jun et al. 2023)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:146,951
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: 559 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 559 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 |
---|---|---|---|---|---|---|---|---|---|
nsv6907486 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 6,769,718 | 6,916,668 | ||
nsv6907486 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 6,790,949 | 6,937,899 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18353130 | deletion | 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 |
---|---|---|---|---|---|---|---|---|---|
nssv18353130 | Submitted genomic | NC_000011.10:g.676 9718_6916668del | GRCh38 (hg38) | NC_000011.10 | Chr11 | 6,769,718 | 6,916,668 | ||
nssv18353130 | Remapped | Perfect | NC_000011.9:g.6790 949_6937899del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 6,790,949 | 6,937,899 |
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) |
---|---|---|---|
nssv18353130 | 7e-06 | 2 | 276152 |