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nsv6727581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,861,742

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 27217 SVs from 125 studies. See in: genome view    
    Submitted genomic28,550,139-38,411,880Question Mark
    Overlapping variant regions from other studies: 27204 SVs from 125 studies. See in: genome view    
    Remapped(Score: Perfect):28,551,761-38,413,501Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6727581Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr428,550,13938,411,880
    nsv6727581RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr428,551,76138,413,501

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18495949deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18495949Submitted genomicNC_000004.12:g.285
    50139_38411880del
    GRCh38 (hg38)NC_000004.12Chr428,550,13938,411,880
    nssv18495949RemappedPerfectNC_000004.11:g.285
    51761_38413501del
    GRCh37.p13First PassNC_000004.11Chr428,551,76138,413,501

    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)
    nssv184959494e-061275866
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