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nsv6816139

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:420,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1718 SVs from 81 studies. See in: genome view    
    Submitted genomic151,077,301-151,497,900Question Mark
    Overlapping variant regions from other studies: 1718 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):151,398,437-151,819,035Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6816139Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6151,077,301151,497,900
    nsv6816139RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6151,398,437151,819,035

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18711540duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18711540Submitted genomicNC_000006.12:g.151
    077301_151497900du
    p
    GRCh38 (hg38)NC_000006.12Chr6151,077,301151,497,900
    nssv18711540RemappedPerfectNC_000006.11:g.151
    398437_151819035du
    p
    GRCh37.p13First PassNC_000006.11Chr6151,398,437151,819,035

    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)
    nssv187115404e-061271912
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