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nsv6742289

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:316,680

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 997 SVs from 82 studies. See in: genome view    
    Submitted genomic67,832,302-68,148,981Question Mark
    Overlapping variant regions from other studies: 997 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):68,698,020-69,014,699Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6742289Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,832,30268,148,981
    nsv6742289RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,698,02069,014,699

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692020duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692020Submitted genomicNC_000004.12:g.678
    32302_68148981dup
    GRCh38 (hg38)NC_000004.12Chr467,832,30268,148,981
    nssv18692020RemappedPerfectNC_000004.11:g.686
    98020_69014699dup
    GRCh37.p13First PassNC_000004.11Chr468,698,02069,014,699

    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)
    nssv186920204e-061275522
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