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nsv7044544

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,220,937

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 21396 SVs from 127 studies. See in: genome view    
    Submitted genomic98,964,941-108,185,877Question Mark
    Overlapping variant regions from other studies: 21424 SVs from 127 studies. See in: genome view    
    Remapped(Score: Perfect):99,886,092-109,107,033Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044544Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr498,964,941108,185,877
    nsv7044544RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr499,886,092109,107,033

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774564inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774564Submitted genomicNC_000004.12:g.989
    64941_108185877inv
    GRCh38 (hg38)NC_000004.12Chr498,964,941108,185,877
    nssv18774564RemappedPerfectNC_000004.11:g.998
    86092_109107033inv
    GRCh37.p13First PassNC_000004.11Chr499,886,092109,107,033

    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)
    nssv18774564<0.00138274160
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