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nsv6391871

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,043

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 36 studies. See in: genome view    
    Submitted genomic67,487,227-67,488,269Question Mark
    Overlapping variant regions from other studies: 138 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):68,352,945-68,353,987Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6391871Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,487,22767,488,269
    nsv6391871RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,352,94568,353,987

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18119467deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18119467Submitted genomicNC_000004.12:g.674
    87227_67488269del
    GRCh38 (hg38)NC_000004.12Chr467,487,22767,488,269
    nssv18119467RemappedPerfectNC_000004.11:g.683
    52945_68353987del
    GRCh37.p13First PassNC_000004.11Chr468,352,94568,353,987

    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)
    nssv181194670.00932538082
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