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nsv7009029

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,353

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 322 SVs from 61 studies. See in: genome view    
    Submitted genomic36,343,834-36,354,186Question Mark
    Overlapping variant regions from other studies: 322 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):36,834,736-36,845,088Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7009029Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,343,83436,354,186
    nsv7009029RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,834,73636,845,088

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423257deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423257Submitted genomicNC_000019.10:g.363
    43834_36354186del
    GRCh38 (hg38)NC_000019.10Chr1936,343,83436,354,186
    nssv18423257RemappedPerfectNC_000019.9:g.3683
    4736_36845088del
    GRCh37.p13First PassNC_000019.9Chr1936,834,73636,845,088

    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)
    nssv184232577e-062271634
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