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nsv7063672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,833

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Submitted genomic97,228,209-97,241,041Question Mark
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):98,240,437-98,253,269Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr897,228,20997,241,041
    nsv7063672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr898,240,43798,253,269

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783578inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783578Submitted genomicNC_000008.11:g.972
    28209_97241041inv
    GRCh38 (hg38)NC_000008.11Chr897,228,20997,241,041
    nssv18783578RemappedPerfectNC_000008.10:g.982
    40437_98253269inv
    GRCh37.p13First PassNC_000008.10Chr898,240,43798,253,269

    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)
    nssv187835784e-061276258
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