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nsv6704071

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:211

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 28 studies. See in: genome view    
    Submitted genomic11,795,081-11,795,291Question Mark
    Overlapping variant regions from other studies: 102 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):11,836,555-11,836,765Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6704071Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,795,08111,795,291
    nsv6704071RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,836,55511,836,765

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18669747duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18669747Submitted genomicNC_000003.12:g.117
    95081_11795291dup
    GRCh38 (hg38)NC_000003.12Chr311,795,08111,795,291
    nssv18669747RemappedPerfectNC_000003.11:g.118
    36555_11836765dup
    GRCh37.p13First PassNC_000003.11Chr311,836,55511,836,765

    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)
    nssv186697478e-062237302
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