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nsv6770792

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:204

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 23 studies. See in: genome view    
    Submitted genomic97,636,896-97,637,099Question Mark
    Overlapping variant regions from other studies: 138 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):96,972,600-96,972,803Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6770792Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr597,636,89697,637,099
    nsv6770792RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr596,972,60096,972,803

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18708306duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18708306Submitted genomicNC_000005.10:g.976
    36896_97637099dup
    GRCh38 (hg38)NC_000005.10Chr597,636,89697,637,099
    nssv18708306RemappedPerfectNC_000005.9:g.9697
    2600_96972803dup
    GRCh37.p13First PassNC_000005.9Chr596,972,60096,972,803

    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)
    nssv187083064e-061237700
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