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nsv6727005

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,628

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 218 SVs from 30 studies. See in: genome view    
    Submitted genomic4,269,007-4,273,634Question Mark
    Overlapping variant regions from other studies: 218 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):4,270,734-4,275,361Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6727005Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr44,269,0074,273,634
    nsv6727005RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr44,270,7344,275,361

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18494672deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18494672Submitted genomicNC_000004.12:g.426
    9007_4273634del
    GRCh38 (hg38)NC_000004.12Chr44,269,0074,273,634
    nssv18494672RemappedPerfectNC_000004.11:g.427
    0734_4275361del
    GRCh37.p13First PassNC_000004.11Chr44,270,7344,275,361

    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)
    nssv184946721.8e-055276028
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