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nsv6993656

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:939,616

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3561 SVs from 110 studies. See in: genome view    
    Submitted genomic80,348,419-81,288,034Question Mark
    Overlapping variant regions from other studies: 3557 SVs from 110 studies. See in: genome view    
    Remapped(Score: Good):80,382,316-81,321,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993656Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1680,348,41981,288,034
    nsv6993656RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1680,382,31681,321,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624692duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624692Submitted genomicNC_000016.10:g.803
    48419_81288034dup
    GRCh38 (hg38)NC_000016.10Chr1680,348,41981,288,034
    nssv18624692RemappedGoodNC_000016.9:g.8038
    2316_81321639dup
    GRCh37.p13First PassNC_000016.9Chr1680,382,31681,321,639

    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)
    nssv186246924e-061274958
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