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nsv6428179

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 21 studies. See in: genome view    
    Submitted genomic56,536,501-56,550,600Question Mark
    Overlapping variant regions from other studies: 142 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):57,449,060-57,463,159Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6428179Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr856,536,50156,550,600
    nsv6428179RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr857,449,06057,463,159

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18169202deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18169202Submitted genomicNC_000008.11:g.565
    36501_56550600del
    GRCh38 (hg38)NC_000008.11Chr856,536,50156,550,600
    nssv18169202RemappedPerfectNC_000008.10:g.574
    49060_57463159del
    GRCh37.p13First PassNC_000008.10Chr857,449,06057,463,159

    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)
    nssv18169202<0.001139272
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