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nsv6912070

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
    Submitted genomic93,417,769-93,417,818Question Mark
    Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):93,150,935-93,150,984Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912070Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1193,417,76993,417,818
    nsv6912070RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1193,150,93593,150,984

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353952deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353952Submitted genomicNC_000011.10:g.934
    17769_93417818del
    GRCh38 (hg38)NC_000011.10Chr1193,417,76993,417,818
    nssv18353952RemappedPerfectNC_000011.9:g.9315
    0935_93150984del
    GRCh37.p13First PassNC_000011.9Chr1193,150,93593,150,984

    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)
    nssv183539521.9e-055261730
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