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nsv6565534

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:663

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Submitted genomic180,885,453-180,886,115Question Mark
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):180,603,241-180,603,903Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6565534Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3180,885,453180,886,115
    nsv6565534RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3180,603,241180,603,903

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18261183inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18261183Submitted genomicNC_000003.12:g.180
    885453_180886115in
    v
    GRCh38 (hg38)NC_000003.12Chr3180,885,453180,886,115
    nssv18261183RemappedPerfectNC_000003.11:g.180
    603241_180603903in
    v
    GRCh37.p13First PassNC_000003.11Chr3180,603,241180,603,903

    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)
    nssv18261183<0.001436120
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