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nsv6922681

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,798

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 28 studies. See in: genome view    
    Submitted genomic91,104,319-91,108,116Question Mark
    Overlapping variant regions from other studies: 112 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):91,498,096-91,501,893Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6922681Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1291,104,31991,108,116
    nsv6922681RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1291,498,09691,501,893

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18374025deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18374025Submitted genomicNC_000012.12:g.911
    04319_91108116del
    GRCh38 (hg38)NC_000012.12Chr1291,104,31991,108,116
    nssv18374025RemappedPerfectNC_000012.11:g.914
    98096_91501893del
    GRCh37.p13First PassNC_000012.11Chr1291,498,09691,501,893

    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)
    nssv183740252.5e-057273454
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