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nsv6714552

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:612,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1314 SVs from 72 studies. See in: genome view    
    Submitted genomic73,824,901-74,437,800Question Mark
    Overlapping variant regions from other studies: 1314 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):73,874,052-74,486,951Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6714552Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr373,824,90174,437,800
    nsv6714552RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr373,874,05274,486,951

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18678862duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18678862Submitted genomicNC_000003.12:g.738
    24901_74437800dup
    GRCh38 (hg38)NC_000003.12Chr373,824,90174,437,800
    nssv18678862RemappedPerfectNC_000003.11:g.738
    74052_74486951dup
    GRCh37.p13First PassNC_000003.11Chr373,874,05274,486,951

    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)
    nssv186788621.1e-053275182
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