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nsv6835343

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:365,747

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1016 SVs from 68 studies. See in: genome view    
    Submitted genomic47,816,930-48,182,676Question Mark
    Overlapping variant regions from other studies: 1016 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):47,856,528-48,222,273Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6835343Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr747,816,93048,182,676
    nsv6835343RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr747,856,52848,222,273

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18726395duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18726395Submitted genomicNC_000007.14:g.478
    16930_48182676dup
    GRCh38 (hg38)NC_000007.14Chr747,816,93048,182,676
    nssv18726395RemappedPerfectNC_000007.13:g.478
    56528_48222273dup
    GRCh37.p13First PassNC_000007.13Chr747,856,52848,222,273

    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)
    nssv187263954e-061275858
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