U.S. flag

An official website of the United States government

nsv7060800

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:905,559

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2116 SVs from 86 studies. See in: genome view    
    Submitted genomic62,887,439-63,792,997Question Mark
    Overlapping variant regions from other studies: 2116 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):62,654,911-63,560,469Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060800Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1162,887,43963,792,997
    nsv7060800RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1162,654,91163,560,469

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739510inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739510Submitted genomicNC_000011.10:g.628
    87439_63792997inv
    GRCh38 (hg38)NC_000011.10Chr1162,887,43963,792,997
    nssv18739510RemappedPerfectNC_000011.9:g.6265
    4911_63560469inv
    GRCh37.p13First PassNC_000011.9Chr1162,654,91163,560,469

    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)
    nssv187395101.4e-054272902
    Support Center