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nsv6723185

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 225 SVs from 40 studies. See in: genome view    
    Submitted genomic55,985,101-56,050,400Question Mark
    Overlapping variant regions from other studies: 225 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):56,851,267-56,916,566Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6723185Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr455,985,10156,050,400
    nsv6723185RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr456,851,26756,916,566

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692832duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692832Submitted genomicNC_000004.12:g.559
    85101_56050400dup
    GRCh38 (hg38)NC_000004.12Chr455,985,10156,050,400
    nssv18692832RemappedPerfectNC_000004.11:g.568
    51267_56916566dup
    GRCh37.p13First PassNC_000004.11Chr456,851,26756,916,566

    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)
    nssv186928324e-061275324
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