U.S. flag

An official website of the United States government

nsv6473220

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,801

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 33 studies. See in: genome view    
    Submitted genomic68,106,991-68,111,791Question Mark
    Overlapping variant regions from other studies: 97 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):67,874,458-67,879,258Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6473220Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1168,106,99168,111,791
    nsv6473220RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,874,45867,879,258

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18190193duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18190193Submitted genomicNC_000011.10:g.681
    06991_68111791dup
    GRCh38 (hg38)NC_000011.10Chr1168,106,99168,111,791
    nssv18190193RemappedPerfectNC_000011.9:g.6787
    4458_67879258dup
    GRCh37.p13First PassNC_000011.9Chr1167,874,45867,879,258

    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)
    nssv18190193<0.001139280
    Support Center