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nsv6967100

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 524 SVs from 63 studies. See in: genome view    
    Submitted genomic100,599,501-100,694,800Question Mark
    Overlapping variant regions from other studies: 524 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):101,139,706-101,235,005Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6967100Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr15100,599,501100,694,800
    nsv6967100RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr15101,139,706101,235,005

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18614917duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18614917Submitted genomicNC_000015.10:g.100
    599501_100694800du
    p
    GRCh38 (hg38)NC_000015.10Chr15100,599,501100,694,800
    nssv18614917RemappedPerfectNC_000015.9:g.1011
    39706_101235005dup
    GRCh37.p13First PassNC_000015.9Chr15101,139,706101,235,005

    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)
    nssv186149174e-061275790
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