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nsv6774450

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:280,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 730 SVs from 62 studies. See in: genome view    
    Submitted genomic31,192,601-31,472,600Question Mark
    Overlapping variant regions from other studies: 730 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):31,192,708-31,472,707Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6774450Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr531,192,60131,472,600
    nsv6774450RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr531,192,70831,472,707

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18703419duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18703419Submitted genomicNC_000005.10:g.311
    92601_31472600dup
    GRCh38 (hg38)NC_000005.10Chr531,192,60131,472,600
    nssv18703419RemappedPerfectNC_000005.9:g.3119
    2708_31472707dup
    GRCh37.p13First PassNC_000005.9Chr531,192,70831,472,707

    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)
    nssv187034198.9e-0513275618
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