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nsv6716752

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 32 studies. See in: genome view    
    Submitted genomic61,871,601-61,881,800Question Mark
    Overlapping variant regions from other studies: 114 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):61,857,275-61,867,474Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6716752Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr361,871,60161,881,800
    nsv6716752RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr361,857,27561,867,474

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18481637deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18481637Submitted genomicNC_000003.12:g.618
    71601_61881800del
    GRCh38 (hg38)NC_000003.12Chr361,871,60161,881,800
    nssv18481637RemappedPerfectNC_000003.11:g.618
    57275_61867474del
    GRCh37.p13First PassNC_000003.11Chr361,857,27561,867,474

    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)
    nssv184816371.1e-053276004
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