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nsv6390223

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,957

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 25 studies. See in: genome view    
    Submitted genomic155,774,619-155,778,575Question Mark
    Overlapping variant regions from other studies: 140 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):156,695,771-156,699,727Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6390223Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4155,774,619155,778,575
    nsv6390223RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4156,695,771156,699,727

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18110263deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18110263Submitted genomicNC_000004.12:g.155
    774619_155778575de
    l
    GRCh38 (hg38)NC_000004.12Chr4155,774,619155,778,575
    nssv18110263RemappedPerfectNC_000004.11:g.156
    695771_156699727de
    l
    GRCh37.p13First PassNC_000004.11Chr4156,695,771156,699,727

    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)
    nssv18110263<0.001139086
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