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nsv6373827

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,919

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 28 studies. See in: genome view    
    Submitted genomic119,548,194-119,561,112Question Mark
    Overlapping variant regions from other studies: 120 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):119,267,041-119,279,959Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6373827Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3119,548,194119,561,112
    nsv6373827RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3119,267,041119,279,959

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18094557deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18094557Submitted genomicNC_000003.12:g.119
    548194_119561112de
    l
    GRCh38 (hg38)NC_000003.12Chr3119,548,194119,561,112
    nssv18094557RemappedPerfectNC_000003.11:g.119
    267041_119279959de
    l
    GRCh37.p13First PassNC_000003.11Chr3119,267,041119,279,959

    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)
    nssv18094557<0.001139262
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