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nsv6941084

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 263 SVs from 45 studies. See in: genome view    
    Submitted genomic45,200,201-45,255,600Question Mark
    Overlapping variant regions from other studies: 263 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):45,774,336-45,829,735Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6941084Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1345,200,20145,255,600
    nsv6941084RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1345,774,33645,829,735

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18604294duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18604294Submitted genomicNC_000013.11:g.452
    00201_45255600dup
    GRCh38 (hg38)NC_000013.11Chr1345,200,20145,255,600
    nssv18604294RemappedPerfectNC_000013.10:g.457
    74336_45829735dup
    GRCh37.p13First PassNC_000013.10Chr1345,774,33645,829,735

    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)
    nssv186042944e-061274896
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