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nsv6970162

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,713

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 48 studies. See in: genome view    
    Submitted genomic4,085,182-4,095,894Question Mark
    Overlapping variant regions from other studies: 190 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):4,135,183-4,145,895Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6970162Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr164,085,1824,095,894
    nsv6970162RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr164,135,1834,145,895

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400955deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400955Submitted genomicNC_000016.10:g.408
    5182_4095894del
    GRCh38 (hg38)NC_000016.10Chr164,085,1824,095,894
    nssv18400955RemappedPerfectNC_000016.9:g.4135
    183_4145895del
    GRCh37.p13First PassNC_000016.9Chr164,135,1834,145,895

    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)
    nssv184009551.1e-053276016
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