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nsv6728046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,112

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 289 SVs from 40 studies. See in: genome view    
    Submitted genomic2,734,575-2,749,686Question Mark
    Overlapping variant regions from other studies: 289 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):2,736,302-2,751,413Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6728046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr42,734,5752,749,686
    nsv6728046RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr42,736,3022,751,413

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18689413duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18689413Submitted genomicNC_000004.12:g.273
    4575_2749686dup
    GRCh38 (hg38)NC_000004.12Chr42,734,5752,749,686
    nssv18689413RemappedPerfectNC_000004.11:g.273
    6302_2751413dup
    GRCh37.p13First PassNC_000004.11Chr42,736,3022,751,413

    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)
    nssv186894131.1e-053274420
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