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nsv6831820

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,278

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 159 SVs from 43 studies. See in: genome view    
    Submitted genomic53,680,557-53,709,834Question Mark
    Overlapping variant regions from other studies: 159 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):53,748,250-53,777,527Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6831820Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr753,680,55753,709,834
    nsv6831820RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr753,748,25053,777,527

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18723737duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18723737Submitted genomicNC_000007.14:g.536
    80557_53709834dup
    GRCh38 (hg38)NC_000007.14Chr753,680,55753,709,834
    nssv18723737RemappedPerfectNC_000007.13:g.537
    48250_53777527dup
    GRCh37.p13First PassNC_000007.13Chr753,748,25053,777,527

    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)
    nssv187237371.8e-055274254
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