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nsv6667187

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,233

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 24 studies. See in: genome view    
    Submitted genomic231,395,711-231,398,943Question Mark
    Overlapping variant regions from other studies: 146 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):231,531,457-231,534,689Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6667187Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,395,711231,398,943
    nsv6667187RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,531,457231,534,689

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18368536deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18368536Submitted genomicNC_000001.11:g.231
    395711_231398943de
    l
    GRCh38 (hg38)NC_000001.11Chr1231,395,711231,398,943
    nssv18368536RemappedPerfectNC_000001.10:g.231
    531457_231534689de
    l
    GRCh37.p13First PassNC_000001.10Chr1231,531,457231,534,689

    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)
    nssv183685364e-061276134
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