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nsv7057436

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:147,239

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 856 SVs from 71 studies. See in: genome view    
    Submitted genomic11,572,735-11,719,973Question Mark
    Overlapping variant regions from other studies: 856 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):11,614,209-11,761,447Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057436Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,572,73511,719,973
    nsv7057436RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,614,20911,761,447

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769238inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769238Submitted genomicNC_000003.12:g.115
    72735_11719973inv
    GRCh38 (hg38)NC_000003.12Chr311,572,73511,719,973
    nssv18769238RemappedPerfectNC_000003.11:g.116
    14209_11761447inv
    GRCh37.p13First PassNC_000003.11Chr311,614,20911,761,447

    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 IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv187692384e-060276268
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