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nsv6558303

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:231,086

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 798 SVs from 79 studies. See in: genome view    
    Submitted genomic155,901,266-156,132,351Question Mark
    Overlapping variant regions from other studies: 798 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):155,328,276-155,559,361Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6558303Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5155,901,266156,132,351
    nsv6558303RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5155,328,276155,559,361

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18268780inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18268780Submitted genomicNC_000005.10:g.155
    901266_156132351in
    v
    GRCh38 (hg38)NC_000005.10Chr5155,901,266156,132,351
    nssv18268780RemappedPerfectNC_000005.9:g.1553
    28276_155559361inv
    GRCh37.p13First PassNC_000005.9Chr5155,328,276155,559,361

    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)
    nssv18268780<0.001139304
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