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nsv6388599

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 26 studies. See in: genome view    
    Submitted genomic86,934,801-86,935,200Question Mark
    Overlapping variant regions from other studies: 139 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):87,855,953-87,856,352Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6388599Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr486,934,80186,935,200
    nsv6388599RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr487,855,95387,856,352

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18121754deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18121754Submitted genomicNC_000004.12:g.869
    34801_86935200del
    GRCh38 (hg38)NC_000004.12Chr486,934,80186,935,200
    nssv18121754RemappedPerfectNC_000004.11:g.878
    55953_87856352del
    GRCh37.p13First PassNC_000004.11Chr487,855,95387,856,352

    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)
    nssv181217540.052194637514
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