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nsv6760940

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:359

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 23 studies. See in: genome view    
    Submitted genomic115,874,760-115,875,118Question Mark
    Overlapping variant regions from other studies: 129 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):115,210,457-115,210,815Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6760940Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,874,760115,875,118
    nsv6760940RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,210,457115,210,815

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18697951duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18697951Submitted genomicNC_000005.10:g.115
    874760_115875118du
    p
    GRCh38 (hg38)NC_000005.10Chr5115,874,760115,875,118
    nssv18697951RemappedPerfectNC_000005.9:g.1152
    10457_115210815dup
    GRCh37.p13First PassNC_000005.9Chr5115,210,457115,210,815

    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)
    nssv18697951<0.00129240784
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