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nsv6557524

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 20 studies. See in: genome view    
    Submitted genomic150,868,216-150,869,015Question Mark
    Overlapping variant regions from other studies: 122 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):150,586,003-150,586,802Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6557524Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3150,868,216150,869,015
    nsv6557524RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3150,586,003150,586,802

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18263207inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18263207Submitted genomicNC_000003.12:g.150
    868216_150869015in
    v
    GRCh38 (hg38)NC_000003.12Chr3150,868,216150,869,015
    nssv18263207RemappedPerfectNC_000003.11:g.150
    586003_150586802in
    v
    GRCh37.p13First PassNC_000003.11Chr3150,586,003150,586,802

    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)
    nssv18263207<0.001135250
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