U.S. flag

An official website of the United States government

nsv7014525

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51,937

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 364 SVs from 61 studies. See in: genome view    
    Submitted genomic20,909,191-20,961,127Question Mark
    Overlapping variant regions from other studies: 361 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):21,091,997-21,143,933Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7014525Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1920,909,19120,961,127
    nsv7014525RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1921,091,99721,143,933

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637330duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637330Submitted genomicNC_000019.10:g.209
    09191_20961127dup
    GRCh38 (hg38)NC_000019.10Chr1920,909,19120,961,127
    nssv18637330RemappedPerfectNC_000019.9:g.2109
    1997_21143933dup
    GRCh37.p13First PassNC_000019.9Chr1921,091,99721,143,933

    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)
    nssv186373307e-062273048
    Support Center