nsv4260460
- 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:12,645
- 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: 75 SVs from 14 studies. See in: genome view
Overlapping variant regions from other studies: 75 SVs from 14 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4260460 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 6,375,477 | 6,388,121 |
nsv4260460 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000019.9 | Chr19 | 6,375,488 | 6,388,132 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15961087 | duplication | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15961087 | Remapped | Perfect | NC_000019.10:g.637 5477_6388121dup | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 6,375,477 | 6,388,121 |
nssv15961087 | Submitted genomic | NC_000019.9:g.6375 488_6388132dup | GRCh37.p13 | NC_000019.9 | Chr19 | 6,375,488 | 6,388,132 |
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) |
---|---|---|---|
nssv15961087 | 0.006 | 125 | 21686 |