nsv4313384
- Organism: Homo sapiens
- Study:nstd166 (gnomAD Structural Variants)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21,499,276
- 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: 17610 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 15313 SVs from 25 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4313384 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 36,819,153 | 58,318,428 |
nsv4313384 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000010.10 | Chr10 | 37,108,081 | 60,078,188 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv16091028 | inversion | Sequencing | Other |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv16091028 | Remapped | Pass | NC_000010.11:g.368 19153_58318428inv | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 36,819,153 | 58,318,428 |
nssv16091028 | Submitted genomic | NC_000010.10:g.371 08081_60078188inv | GRCh37.p13 | NC_000010.10 | Chr10 | 37,108,081 | 60,078,188 |
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) |
---|---|---|---|
nssv16091028 | <0.001 | 3 | 21694 |