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nsv6772810

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 161 SVs from 29 studies. See in: genome view    
    Submitted genomic78,757,601-78,781,200Question Mark
    Overlapping variant regions from other studies: 161 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):78,053,424-78,077,023Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6772810Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr578,757,60178,781,200
    nsv6772810RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr578,053,42478,077,023

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18707534duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18707534Submitted genomicNC_000005.10:g.787
    57601_78781200dup
    GRCh38 (hg38)NC_000005.10Chr578,757,60178,781,200
    nssv18707534RemappedPerfectNC_000005.9:g.7805
    3424_78077023dup
    GRCh37.p13First PassNC_000005.9Chr578,053,42478,077,023

    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)
    nssv187075344e-061275206
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