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nsv6979633

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,605

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 21 studies. See in: genome view    
    Submitted genomic77,970,022-77,981,626Question Mark
    Overlapping variant regions from other studies: 139 SVs from 21 studies. See in: genome view    
    Remapped(Score: Good):75,966,104-75,977,707Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6979633Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1777,970,02277,981,626
    nsv6979633RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1775,966,10475,977,707

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413324deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413324Submitted genomicNC_000017.11:g.779
    70022_77981626del
    GRCh38 (hg38)NC_000017.11Chr1777,970,02277,981,626
    nssv18413324RemappedGoodNC_000017.10:g.759
    66104_75977707del
    GRCh37.p13First PassNC_000017.10Chr1775,966,10475,977,707

    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)
    nssv184133244e-061276240
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