U.S. flag

An official website of the United States government

nsv7039558

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,169,920

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7271 SVs from 101 studies. See in: genome view    
    Submitted genomic155,298,171-158,468,090Question Mark
    Overlapping variant regions from other studies: 7278 SVs from 101 studies. See in: genome view    
    Remapped(Score: Perfect):155,267,962-158,437,880Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039558Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,298,171158,468,090
    nsv7039558RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1155,267,962158,437,880

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747924inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747924Submitted genomicNC_000001.11:g.155
    298171_158468090in
    v
    GRCh38 (hg38)NC_000001.11Chr1155,298,171158,468,090
    nssv18747924RemappedPerfectNC_000001.10:g.155
    267962_158437880in
    v
    GRCh37.p13First PassNC_000001.10Chr1155,267,962158,437,880

    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)
    nssv187479247e-062272366
    Support Center