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nsv6563275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:227,173

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 922 SVs from 76 studies. See in: genome view    
    Submitted genomic142,782,774-143,009,946Question Mark
    Overlapping variant regions from other studies: 887 SVs from 81 studies. See in: genome view    
    Remapped(Score: Good):142,490,584-142,707,033Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6563275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7142,782,774143,009,946
    nsv6563275RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7142,490,584142,707,033

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18274505inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18274505Submitted genomicNC_000007.14:g.142
    782774_143009946in
    v
    GRCh38 (hg38)NC_000007.14Chr7142,782,774143,009,946
    nssv18274505RemappedGoodNC_000007.13:g.142
    490584_142707033in
    v
    GRCh37.p13First PassNC_000007.13Chr7142,490,584142,707,033

    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)
    nssv18274505<0.001239304
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