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nsv6560897

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:635,182

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1753 SVs from 85 studies. See in: genome view    
    Submitted genomic136,184,622-136,819,803Question Mark
    Overlapping variant regions from other studies: 1753 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):135,903,464-136,538,645Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6560897Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3136,184,622136,819,803
    nsv6560897RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3135,903,464136,538,645

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18260308inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18260308Submitted genomicNC_000003.12:g.136
    184622_136819803in
    v
    GRCh38 (hg38)NC_000003.12Chr3136,184,622136,819,803
    nssv18260308RemappedPerfectNC_000003.11:g.135
    903464_136538645in
    v
    GRCh37.p13First PassNC_000003.11Chr3135,903,464136,538,645

    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)
    nssv18260308<0.001139304
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