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nsv6977657

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:407,736

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1919 SVs from 94 studies. See in: genome view    
    Submitted genomic100,373,283-100,781,018Question Mark
    Overlapping variant regions from other studies: 1919 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):100,913,488-101,321,223Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977657Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr15100,373,283100,781,018
    nsv6977657RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr15100,913,488101,321,223

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18614908duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18614908Submitted genomicNC_000015.10:g.100
    373283_100781018du
    p
    GRCh38 (hg38)NC_000015.10Chr15100,373,283100,781,018
    nssv18614908RemappedPerfectNC_000015.9:g.1009
    13488_101321223dup
    GRCh37.p13First PassNC_000015.9Chr15100,913,488101,321,223

    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)
    nssv186149084e-061275398
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