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nsv6749863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:573,363

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1783 SVs from 88 studies. See in: genome view    
    Submitted genomic64,629,981-65,203,343Question Mark
    Overlapping variant regions from other studies: 1783 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):65,495,699-66,069,061Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6749863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr464,629,98165,203,343
    nsv6749863RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr465,495,69966,069,061

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692573duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692573Submitted genomicNC_000004.12:g.646
    29981_65203343dup
    GRCh38 (hg38)NC_000004.12Chr464,629,98165,203,343
    nssv18692573RemappedPerfectNC_000004.11:g.654
    95699_66069061dup
    GRCh37.p13First PassNC_000004.11Chr465,495,69966,069,061

    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)
    nssv186925734e-061274864
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