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nsv6741348

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:103,697

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 488 SVs from 64 studies. See in: genome view    
    Submitted genomic67,374,723-67,478,419Question Mark
    Overlapping variant regions from other studies: 488 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):68,240,441-68,344,137Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6741348Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,374,72367,478,419
    nsv6741348RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,240,44168,344,137

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18691992duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18691992Submitted genomicNC_000004.12:g.673
    74723_67478419dup
    GRCh38 (hg38)NC_000004.12Chr467,374,72367,478,419
    nssv18691992RemappedPerfectNC_000004.11:g.682
    40441_68344137dup
    GRCh37.p13First PassNC_000004.11Chr468,240,44168,344,137

    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)
    nssv186919929.6e-0527275626
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