U.S. flag

An official website of the United States government

nsv6531854

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:757

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
    Submitted genomic36,413,917-36,414,673Question Mark
    Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):36,904,819-36,905,575Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6531854Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,413,91736,414,673
    nsv6531854RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,904,81936,905,575

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18046154deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18046154Submitted genomicNC_000019.10:g.364
    13917_36414673del
    GRCh38 (hg38)NC_000019.10Chr1936,413,91736,414,673
    nssv18046154RemappedPerfectNC_000019.9:g.3690
    4819_36905575del
    GRCh37.p13First PassNC_000019.9Chr1936,904,81936,905,575

    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)
    nssv18046154<0.001335936
    Support Center