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nsv7000496

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 17 studies. See in: genome view    
    Submitted genomic37,896,701-37,897,821Question Mark
    Overlapping variant regions from other studies: 119 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):38,387,341-38,388,461Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7000496Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1937,896,70137,897,821
    nsv7000496RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1938,387,34138,388,461

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637934duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637934Submitted genomicNC_000019.10:g.378
    96701_37897821dup
    GRCh38 (hg38)NC_000019.10Chr1937,896,70137,897,821
    nssv18637934RemappedPerfectNC_000019.9:g.3838
    7341_38388461dup
    GRCh37.p13First PassNC_000019.9Chr1938,387,34138,388,461

    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)
    nssv186379344e-061253154
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