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nsv6911304

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,140

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Submitted genomic106,258,362-106,263,501Question Mark
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):106,129,089-106,134,228Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6911304Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11106,258,362106,263,501
    nsv6911304RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11106,129,089106,134,228

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581563duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581563Submitted genomicNC_000011.10:g.106
    258362_106263501du
    p
    GRCh38 (hg38)NC_000011.10Chr11106,258,362106,263,501
    nssv18581563RemappedPerfectNC_000011.9:g.1061
    29089_106134228dup
    GRCh37.p13First PassNC_000011.9Chr11106,129,089106,134,228

    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)
    nssv185815634e-061274558
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