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nsv6999792

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:121,948

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 451 SVs from 56 studies. See in: genome view    
    Submitted genomic36,044,743-36,166,690Question Mark
    Overlapping variant regions from other studies: 451 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):36,535,645-36,657,592Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6999792Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,044,74336,166,690
    nsv6999792RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,535,64536,657,592

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637837duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637837Submitted genomicNC_000019.10:g.360
    44743_36166690dup
    GRCh38 (hg38)NC_000019.10Chr1936,044,74336,166,690
    nssv18637837RemappedPerfectNC_000019.9:g.3653
    5645_36657592dup
    GRCh37.p13First PassNC_000019.9Chr1936,535,64536,657,592

    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)
    nssv186378374e-061275710
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