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nsv6984063

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,742

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 28 studies. See in: genome view    
    Submitted genomic56,905,338-56,918,079Question Mark
    Overlapping variant regions from other studies: 128 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):56,939,250-56,951,991Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6984063Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1656,905,33856,918,079
    nsv6984063RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1656,939,25056,951,991

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18623944duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18623944Submitted genomicNC_000016.10:g.569
    05338_56918079dup
    GRCh38 (hg38)NC_000016.10Chr1656,905,33856,918,079
    nssv18623944RemappedPerfectNC_000016.9:g.5693
    9250_56951991dup
    GRCh37.p13First PassNC_000016.9Chr1656,939,25056,951,991

    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)
    nssv186239444e-061275870
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