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nsv6705914

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,608

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 30 studies. See in: genome view    
    Submitted genomic11,760,810-11,766,417Question Mark
    Overlapping variant regions from other studies: 113 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):11,802,284-11,807,891Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6705914Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,760,81011,766,417
    nsv6705914RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,802,28411,807,891

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18669721duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18669721Submitted genomicNC_000003.12:g.117
    60810_11766417dup
    GRCh38 (hg38)NC_000003.12Chr311,760,81011,766,417
    nssv18669721RemappedPerfectNC_000003.11:g.118
    02284_11807891dup
    GRCh37.p13First PassNC_000003.11Chr311,802,28411,807,891

    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)
    nssv186697214e-061272866
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