nsv4527131
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:694
- Publication(s):gnomAD_Structural_Variants
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: 35 SVs from 5 studies. See in: genome view
Overlapping variant regions from other studies: 35 SVs from 5 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4527131 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 65,622,625 | 65,623,318 |
nsv4527131 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000008.10 | Chr8 | 66,534,860 | 66,535,553 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15926445 | deletion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15926445 | Remapped | Perfect | NC_000008.11:g.656 22625_65623318del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 65,622,625 | 65,623,318 |
nssv15926445 | Submitted genomic | NC_000008.10:g.665 34860_66535553del | GRCh37.p13 | NC_000008.10 | Chr8 | 66,534,860 | 66,535,553 |
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) |
---|---|---|---|
nssv15926445 | 9.3e-005 | 2 | 21590 |