U.S. flag

An official website of the United States government

nsv7053035

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,149

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 30 studies. See in: genome view    
    Submitted genomic133,341,287-133,352,435Question Mark
    Overlapping variant regions from other studies: 112 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):132,676,979-132,688,127Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5133,341,287133,352,435
    nsv7053035RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5132,676,979132,688,127

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775339inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775339Submitted genomicNC_000005.10:g.133
    341287_133352435in
    v
    GRCh38 (hg38)NC_000005.10Chr5133,341,287133,352,435
    nssv18775339RemappedPerfectNC_000005.9:g.1326
    76979_132688127inv
    GRCh37.p13First PassNC_000005.9Chr5132,676,979132,688,127

    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)
    nssv18775339<0.00136273950
    Support Center