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nsv7074373

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:126

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 23 studies. See in: genome view    
    Submitted genomic44,453,279-44,453,404Question Mark
    Overlapping variant regions from other studies: 101 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):44,745,477-44,745,602Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074373Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1544,453,27944,453,404
    nsv7074373RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1544,745,47744,745,602

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754792inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754792Submitted genomicNC_000015.10:g.444
    53279_44453404inv
    GRCh38 (hg38)NC_000015.10Chr1544,453,27944,453,404
    nssv18754792RemappedPerfectNC_000015.9:g.4474
    5477_44745602inv
    GRCh37.p13First PassNC_000015.9Chr1544,745,47744,745,602

    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)
    nssv18754792<0.001107272586
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