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nsv6716746

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 27 studies. See in: genome view    
    Submitted genomic52,390,601-52,394,000Question Mark
    Overlapping variant regions from other studies: 104 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):52,424,617-52,428,016Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6716746Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr352,390,60152,394,000
    nsv6716746RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr352,424,61752,428,016

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18482900deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18482900Submitted genomicNC_000003.12:g.523
    90601_52394000del
    GRCh38 (hg38)NC_000003.12Chr352,390,60152,394,000
    nssv18482900RemappedPerfectNC_000003.11:g.524
    24617_52428016del
    GRCh37.p13First PassNC_000003.11Chr352,424,61752,428,016

    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)
    nssv184829001.8e-055272190
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