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nsv6757052

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:325,686

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 851 SVs from 74 studies. See in: genome view    
    Submitted genomic114,623,166-114,948,851Question Mark
    Overlapping variant regions from other studies: 851 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):115,544,322-115,870,007Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6757052Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4114,623,166114,948,851
    nsv6757052RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4115,544,322115,870,007

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18682143duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18682143Submitted genomicNC_000004.12:g.114
    623166_114948851du
    p
    GRCh38 (hg38)NC_000004.12Chr4114,623,166114,948,851
    nssv18682143RemappedPerfectNC_000004.11:g.115
    544322_115870007du
    p
    GRCh37.p13First PassNC_000004.11Chr4115,544,322115,870,007

    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)
    nssv186821434e-061273688
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