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nsv6930180

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 210 SVs from 44 studies. See in: genome view    
    Submitted genomic27,619,923-27,619,991Question Mark
    Overlapping variant regions from other studies: 210 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):27,772,856-27,772,924Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930180Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1227,619,92327,619,991
    nsv6930180RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1227,772,85627,772,924

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18596663duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18596663Submitted genomicNC_000012.12:g.276
    19923_27619991dup
    GRCh38 (hg38)NC_000012.12Chr1227,619,92327,619,991
    nssv18596663RemappedPerfectNC_000012.11:g.277
    72856_27772924dup
    GRCh37.p13First PassNC_000012.11Chr1227,772,85627,772,924

    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)
    nssv18596663<0.001100213482
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