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nsv6393022

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 205 SVs from 32 studies. See in: genome view    
    Submitted genomic176,318,201-176,320,900Question Mark
    Overlapping variant regions from other studies: 205 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):177,239,352-177,242,051Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6393022Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4176,318,201176,320,900
    nsv6393022RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4177,239,352177,242,051

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18212782duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18212782Submitted genomicNC_000004.12:g.176
    318201_176320900du
    p
    GRCh38 (hg38)NC_000004.12Chr4176,318,201176,320,900
    nssv18212782RemappedPerfectNC_000004.11:g.177
    239352_177242051du
    p
    GRCh37.p13First PassNC_000004.11Chr4177,239,352177,242,051

    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)
    nssv18212782<0.001438338
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