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nsv6745238

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,893

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 29 studies. See in: genome view    
    Submitted genomic67,707,742-67,715,634Question Mark
    Overlapping variant regions from other studies: 127 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):68,573,460-68,581,352Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6745238Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,707,74267,715,634
    nsv6745238RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,573,46068,581,352

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692014duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692014Submitted genomicNC_000004.12:g.677
    07742_67715634dup
    GRCh38 (hg38)NC_000004.12Chr467,707,74267,715,634
    nssv18692014RemappedPerfectNC_000004.11:g.685
    73460_68581352dup
    GRCh37.p13First PassNC_000004.11Chr468,573,46068,581,352

    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)
    nssv186920141.4e-054275274
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