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nsv6977805

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 294 SVs from 40 studies. See in: genome view    
    Submitted genomic91,486,001-91,541,400Question Mark
    Overlapping variant regions from other studies: 289 SVs from 40 studies. See in: genome view    
    Remapped(Score: Pass):91,952,345-92,002,208Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977805Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1491,486,00191,541,400
    nsv6977805RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1491,952,34592,002,208

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615392duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615392Submitted genomicNC_000014.9:g.9148
    6001_91541400dup
    GRCh38 (hg38)NC_000014.9Chr1491,486,00191,541,400
    nssv18615392RemappedPassNC_000014.8:g.9195
    2345_92002208dup
    GRCh37.p13First PassNC_000014.8Chr1491,952,34592,002,208

    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)
    nssv186153924e-061274662
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