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nsv6769530

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,226

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 18 studies. See in: genome view    
    Submitted genomic76,489,872-76,496,097Question Mark
    Overlapping variant regions from other studies: 91 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):75,785,697-75,791,922Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6769530Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr576,489,87276,496,097
    nsv6769530RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr575,785,69775,791,922

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18706954duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18706954Submitted genomicNC_000005.10:g.764
    89872_76496097dup
    GRCh38 (hg38)NC_000005.10Chr576,489,87276,496,097
    nssv18706954RemappedPerfectNC_000005.9:g.7578
    5697_75791922dup
    GRCh37.p13First PassNC_000005.9Chr575,785,69775,791,922

    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)
    nssv187069544e-061275808
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