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nsv6566043

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:520

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view    
    Submitted genomic165,409,306-165,409,825Question Mark
    Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):166,330,458-166,330,977Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6566043Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4165,409,306165,409,825
    nsv6566043RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4166,330,458166,330,977

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18264931inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18264931Submitted genomicNC_000004.12:g.165
    409306_165409825in
    v
    GRCh38 (hg38)NC_000004.12Chr4165,409,306165,409,825
    nssv18264931RemappedPerfectNC_000004.11:g.166
    330458_166330977in
    v
    GRCh37.p13First PassNC_000004.11Chr4166,330,458166,330,977

    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)
    nssv18264931<0.001136288
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