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nsv6891047

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,001,576

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2628 SVs from 85 studies. See in: genome view    
    Submitted genomic9,379,303-10,380,878Question Mark
    Overlapping variant regions from other studies: 2628 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):9,421,266-10,422,841Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6891047Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr109,379,30310,380,878
    nsv6891047RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr109,421,26610,422,841

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18588034duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18588034Submitted genomicNC_000010.11:g.937
    9303_10380878dup
    GRCh38 (hg38)NC_000010.11Chr109,379,30310,380,878
    nssv18588034RemappedPerfectNC_000010.10:g.942
    1266_10422841dup
    GRCh37.p13First PassNC_000010.10Chr109,421,26610,422,841

    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)
    nssv185880344e-061275656
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