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nsv6935087

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:876,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2706 SVs from 106 studies. See in: genome view    
    Submitted genomic26,967,401-27,843,600Question Mark
    Overlapping variant regions from other studies: 2706 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):27,120,334-27,996,533Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6935087Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1226,967,40127,843,600
    nsv6935087RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1227,120,33427,996,533

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18596611duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18596611Submitted genomicNC_000012.12:g.269
    67401_27843600dup
    GRCh38 (hg38)NC_000012.12Chr1226,967,40127,843,600
    nssv18596611RemappedPerfectNC_000012.11:g.271
    20334_27996533dup
    GRCh37.p13First PassNC_000012.11Chr1227,120,33427,996,533

    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)
    nssv18596611<0.00162265784
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