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nsv6857941

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:287,057

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 700 SVs from 73 studies. See in: genome view    
    Submitted genomic55,411,549-55,698,605Question Mark
    Overlapping variant regions from other studies: 700 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):56,324,109-56,611,164Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6857941Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr855,411,54955,698,605
    nsv6857941RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr856,324,10956,611,164

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738550duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738550Submitted genomicNC_000008.11:g.554
    11549_55698605dup
    GRCh38 (hg38)NC_000008.11Chr855,411,54955,698,605
    nssv18738550RemappedPerfectNC_000008.10:g.563
    24109_56611164dup
    GRCh37.p13First PassNC_000008.10Chr856,324,10956,611,164

    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)
    nssv187385504e-061275706
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