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nsv6912527

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:387,495

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1319 SVs from 93 studies. See in: genome view    
    Submitted genomic3,129,375-3,516,869Question Mark
    Overlapping variant regions from other studies: 1319 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):3,150,605-3,538,099Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912527Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr113,129,3753,516,869
    nsv6912527RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr113,150,6053,538,099

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18587273duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18587273Submitted genomicNC_000011.10:g.312
    9375_3516869dup
    GRCh38 (hg38)NC_000011.10Chr113,129,3753,516,869
    nssv18587273RemappedPerfectNC_000011.9:g.3150
    605_3538099dup
    GRCh37.p13First PassNC_000011.9Chr113,150,6053,538,099

    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)
    nssv185872734e-061274170
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