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nsv6849806

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:272,816

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 815 SVs from 61 studies. See in: genome view    
    Submitted genomic67,191,086-67,463,901Question Mark
    Overlapping variant regions from other studies: 815 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):68,103,321-68,376,136Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6849806Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr867,191,08667,463,901
    nsv6849806RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr868,103,32168,376,136

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18745122duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18745122Submitted genomicNC_000008.11:g.671
    91086_67463901dup
    GRCh38 (hg38)NC_000008.11Chr867,191,08667,463,901
    nssv18745122RemappedPerfectNC_000008.10:g.681
    03321_68376136dup
    GRCh37.p13First PassNC_000008.10Chr868,103,32168,376,136

    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)
    nssv187451224e-061274178
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