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nsv6835608

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,015,215

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3369 SVs from 94 studies. See in: genome view    
    Submitted genomic65,825,345-66,840,559Question Mark
    Overlapping variant regions from other studies: 3352 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):65,290,332-66,305,546Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6835608Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr765,825,34566,840,559
    nsv6835608RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr765,290,33266,305,546

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18728527duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18728527Submitted genomicNC_000007.14:g.658
    25345_66840559dup
    GRCh38 (hg38)NC_000007.14Chr765,825,34566,840,559
    nssv18728527RemappedPerfectNC_000007.13:g.652
    90332_66305546dup
    GRCh37.p13First PassNC_000007.13Chr765,290,33266,305,546

    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)
    nssv187285274e-061276050
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