nsv5475971
- Organism: Homo sapiens
- Study:nstd206 (Byrska-Bishop et al. 2022)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:13,454
- Publication(s):Byrska-Bishop et al. 2022
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: 268 SVs from 39 studies. See in: genome view
Overlapping variant regions from other studies: 269 SVs from 39 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5475971 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 127,704,200 | 127,717,653 | ||
nsv5475971 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 128,716,445 | 128,729,899 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17016419 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17016419 | Submitted genomic | NC_000008.11:g.127 704200_127717653de l | GRCh38 (hg38) | NC_000008.11 | Chr8 | 127,704,200 | 127,717,653 | ||
nssv17016419 | Remapped | Good | NC_000008.10:g.128 716445_128729899de l | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 128,716,445 | 128,729,899 |
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) |
---|---|---|---|
nssv17016419 | <0.001 | 2 | 6404 |