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nsv6793334

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 317 SVs from 54 studies. See in: genome view    
    Submitted genomic75,167,901-75,266,600Question Mark
    Overlapping variant regions from other studies: 317 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):75,877,617-75,976,316Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793334Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr675,167,90175,266,600
    nsv6793334RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr675,877,61775,976,316

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18718129duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18718129Submitted genomicNC_000006.12:g.751
    67901_75266600dup
    GRCh38 (hg38)NC_000006.12Chr675,167,90175,266,600
    nssv18718129RemappedPerfectNC_000006.11:g.758
    77617_75976316dup
    GRCh37.p13First PassNC_000006.11Chr675,877,61775,976,316

    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)
    nssv187181297e-062273844
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