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nsv6946735

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157 SVs from 22 studies. See in: genome view    
    Submitted genomic95,513,615-95,513,688Question Mark
    Overlapping variant regions from other studies: 157 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):96,165,869-96,165,942Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6946735Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1395,513,61595,513,688
    nsv6946735RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1396,165,86996,165,942

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611455duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611455Submitted genomicNC_000013.11:g.955
    13615_95513688dup
    GRCh38 (hg38)NC_000013.11Chr1395,513,61595,513,688
    nssv18611455RemappedPerfectNC_000013.10:g.961
    65869_96165942dup
    GRCh37.p13First PassNC_000013.10Chr1396,165,86996,165,942

    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)
    nssv186114550.0265726213156
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