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nsv6763127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,585

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
    Submitted genomic95,710,508-95,715,092Question Mark
    Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):95,046,212-95,050,796Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6763127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr595,710,50895,715,092
    nsv6763127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr595,046,21295,050,796

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18708176duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18708176Submitted genomicNC_000005.10:g.957
    10508_95715092dup
    GRCh38 (hg38)NC_000005.10Chr595,710,50895,715,092
    nssv18708176RemappedPerfectNC_000005.9:g.9504
    6212_95050796dup
    GRCh37.p13First PassNC_000005.9Chr595,046,21295,050,796

    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)
    nssv187081764e-061275624
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