U.S. flag

An official website of the United States government

nsv6444091

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:814

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 77 SVs from 18 studies. See in: genome view    
    Submitted genomic68,986,214-68,987,027Question Mark
    Overlapping variant regions from other studies: 77 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):70,745,970-70,746,783Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6444091Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1068,986,21468,987,027
    nsv6444091RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1070,745,97070,746,783

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17983056deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17983056Submitted genomicNC_000010.11:g.689
    86214_68987027del
    GRCh38 (hg38)NC_000010.11Chr1068,986,21468,987,027
    nssv17983056RemappedPerfectNC_000010.10:g.707
    45970_70746783del
    GRCh37.p13First PassNC_000010.10Chr1070,745,97070,746,783

    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)
    nssv17983056<0.001130502
    Support Center