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nsv7016629

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 67 SVs from 21 studies. See in: genome view    
    Submitted genomic49,308,301-49,310,900Question Mark
    Overlapping variant regions from other studies: 67 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):49,811,558-49,814,157Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7016629Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1949,308,30149,310,900
    nsv7016629RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,811,55849,814,157

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18424102deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18424102Submitted genomicNC_000019.10:g.493
    08301_49310900del
    GRCh38 (hg38)NC_000019.10Chr1949,308,30149,310,900
    nssv18424102RemappedPerfectNC_000019.9:g.4981
    1558_49814157del
    GRCh37.p13First PassNC_000019.9Chr1949,811,55849,814,157

    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)
    nssv184241024e-061252834
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