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nsv6701779

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,765

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 162 SVs from 29 studies. See in: genome view    
    Submitted genomic9,923,511-9,929,275Question Mark
    Overlapping variant regions from other studies: 162 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):9,965,195-9,970,959Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6701779Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr39,923,5119,929,275
    nsv6701779RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr39,965,1959,970,959

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18681466duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18681466Submitted genomicNC_000003.12:g.992
    3511_9929275dup
    GRCh38 (hg38)NC_000003.12Chr39,923,5119,929,275
    nssv18681466RemappedPerfectNC_000003.11:g.996
    5195_9970959dup
    GRCh37.p13First PassNC_000003.11Chr39,965,1959,970,959

    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)
    nssv186814664e-061275462
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