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nsv6575575

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:389

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
    Submitted genomic109,676,102-109,676,490Question Mark
    Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):110,597,258-110,597,646Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6575575Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4109,676,102109,676,490
    nsv6575575RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4110,597,258110,597,646

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18263561inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18263561Submitted genomicNC_000004.12:g.109
    676102_109676490in
    v
    GRCh38 (hg38)NC_000004.12Chr4109,676,102109,676,490
    nssv18263561RemappedPerfectNC_000004.11:g.110
    597258_110597646in
    v
    GRCh37.p13First PassNC_000004.11Chr4110,597,258110,597,646

    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)
    nssv18263561<0.001533314
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