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nsv6534466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,183

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
    Submitted genomic29,520,756-29,524,938Question Mark
    Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):30,011,663-30,015,845Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6534466Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1929,520,75629,524,938
    nsv6534466RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1930,011,66330,015,845

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18047477deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18047477Submitted genomicNC_000019.10:g.295
    20756_29524938del
    GRCh38 (hg38)NC_000019.10Chr1929,520,75629,524,938
    nssv18047477RemappedPerfectNC_000019.9:g.3001
    1663_30015845del
    GRCh37.p13First PassNC_000019.9Chr1930,011,66330,015,845

    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)
    nssv18047477<0.001239098
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