nsv4055085
- 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:25,585
- 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 9 studies. See in: genome view
Overlapping variant regions from other studies: 35 SVs from 9 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4055085 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 62,508,720 | 62,534,304 |
nsv4055085 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000002.11 | Chr2 | 62,735,855 | 62,761,439 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15870363 | deletion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15870363 | Remapped | Perfect | NC_000002.12:g.625 08720_62534304del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 62,508,720 | 62,534,304 |
nssv15870363 | Submitted genomic | NC_000002.11:g.627 35855_62761439del | GRCh37.p13 | NC_000002.11 | Chr2 | 62,735,855 | 62,761,439 |
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) |
---|---|---|---|
nssv15870363 | <0.001 | 5 | 21694 |