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nsv6983444

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 289 SVs from 64 studies. See in: genome view    
    Submitted genomic86,234,301-86,266,700Question Mark
    Overlapping variant regions from other studies: 289 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):86,267,907-86,300,306Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6983444Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1686,234,30186,266,700
    nsv6983444RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1686,267,90786,300,306

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18406457deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18406457Submitted genomicNC_000016.10:g.862
    34301_86266700del
    GRCh38 (hg38)NC_000016.10Chr1686,234,30186,266,700
    nssv18406457RemappedPerfectNC_000016.9:g.8626
    7907_86300306del
    GRCh37.p13First PassNC_000016.9Chr1686,267,90786,300,306

    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)
    nssv18406457<0.00153253762
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